JP4971440B2 - Surgical implants, tools, and methods for treating pelvic disease - Google Patents

Description

(Claiming priority)
This application was filed on Patent Document 1 filed on June 16, 2006 entitled “PELVIC FLOOR REPAIR TISSUE FIXATION” and on January 26, 2007 named “ARM LENGTH REDUCTION / TENSIONING CONCEPT”. Claiming priority based on Patent Document 2.

  The present invention relates to an apparatus and method for treating pelvic disease using a pelvic implant to support pelvic tissue. Pelvic diseases include anatomical illnesses in women or men, especially the treatment of female or male urine and stool incontinence and intestinal aneurysms, rectal aneurysms, cystoceles, decapitation, and symptoms thereof Treatment of female vaginal prolapse, including any combination of. Particular examples of the articles and tools described herein include implants that support pelvic tissue and that can be adjusted surgically and with adjustable length and tension during or after implantation; And an implantable tool with various shapes.

  Men's and women's pelvic health is a medical field of increasing importance, at least in part due to aging. Examples of common pelvic diseases include incontinence (stool and urine) and pelvic tissue prolapse (eg, female vaginal prolapse). Urinary incontinence is further subdivided and includes various types, such as stress urinary incontinence (SUI), urge urinary incontinence, mixed urinary incontinence and the like. Other pelvic bed abnormalities include cystocele, rectal aneurysms, intestinal aneurysms, and prolapses such as anus, uterus, vaginal vault. A cystocele is a hernia of the bladder, usually into the vagina and vaginal opening. These pelvic abnormalities can occur as a result of weakness or damage to the normal pelvic support system.

  In its most severe form, vaginal prolapse can result in a fullness of the vaginal apex outside the vagina. An intestinal aneurysm is a vaginal hernia in which a peritoneal sac that houses part of the small intestine extends into the rectal and vaginal spaces. Vaginal fornix and intestinal aneurysm represent a form of pelvic abnormalities that are challenging for surgeons. These operations often require lengthy surgical procedures.

  Urinary incontinence is characterized by a loss or decrease in the ability to keep the urethral sphincter closed when the bladder is full of urine. Male or female stress urinary incontinence (SUI) occurs when a patient is physically exposed to stress.

  One cause of urinary incontinence is damage to the urethral sphincter. Other causes include loss of urethral sphincter support, such as those occurring in men after prostatectomy or postoperative radiation therapy, pelvic accidents, and support for the urethra Including those caused by age-related degradation of muscles and connective tissue. Other male incontinence causes include unstable bladder, overflow urinary incontinence, and fistulas.

  The natural support system of the female urethra is a hammock-like support layer composed of endopelvic fascia, anterior vaginal wall, and tendon arch. Weakness and elongation of the pubic urethral ligament and pelvic fascia tendon, as well as weakening of the pelvic fascia and pubic urethral prolapse of the vaginal wall, contribute to loss of pelvic support for the urethra and anatomy leading to urinary incontinence Can result in low and low positions.

  In general, urinary self-control is thought to be a function of urethral support and bonding. In order to be effective in preventing or treating incontinence, the urethra must be supported and stabilized in its normal anatomical position. Numerous surgical and implantable medical devices have been developed over the years to provide urethral support and restore bonding. Embodiments of such surgical instruments include a Stamay needle, a Raz needle, and a Pereyra needle. See Non-Patent Document 1 and Non-Patent Document 2.

  Another surgical operation is a pubic vaginal sling operation. A pubic-vaginal sling procedure is a surgical procedure that involves the placement of a sling to stabilize or support the bladder neck or urethra. There are a variety of different sling procedures. Descriptions of the different sling procedures can be found in US Pat.

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Stamey: “Endoscopic Suspension of the Vessel Neck for Urinary Incontinence in Females” (Ann. Surgery, pp. 465-471, October 1980) Pereyra: “A Simply Surgical Procedure for the Correction of Stress In Continence in Women” (West. J. Surg., Obstrics & Gynecology, pp. 243-346)

  Some pubic vaginal sling procedures extend the sling from the rectal fascia in the abdominal region to a position below the urethra and vice versa. The sling comprises a central portion (ie, “support portion” or “tissue support portion”) adapted to support an organ of the urethra or pelvis and two extension portions that support the support portion, optionally at least One or more protective sheaths wrap around the extension. Complications associated with sling surgery occur, albeit rarely. Complications include urethral obstruction, prolonged urine retention, bladder perforation, damage to surrounding tissue, and sling fistulas.

  Other treatments include a Kaufman Prosthesis transplant, an artificial sphincter (such as the AMS-800 Urine Primary Control System available from American Medical Systems, Inc.), or a urethral sling inserted under the urethra. Includes urethral sling surgery that extends to the posterior part. The periphery or extension of the elongated urethral sling is secured to bone or body tissue at or near the posterior pubic area. The central support portion of the elongated urethral sling extends below the urethra or bladder neck to form a platform that compresses the urethral sphincter, limiting urethral dilation and pelvic drooping, thereby improving connectivity To do. Similar wearable slings or supports have been proposed to restore proper placement of pelvic organs, such as the vagina and bladder.

  Elongated “self-fixing” slings have also been introduced for implantation into the body to treat pelvic illnesses such as prolapse and incontinence. Self-fixing slings do not require an extension to physically attach to tissue or bone. Rather, the sling relies on the growth of tissue within the sling pores to stabilize the sling. For example, see Patent Literature 11, Patent Literature 12, Patent Literature 13, and Patent Literature 14 assigned to the same assignee as the present applicant, and literature and patents cited in these specifications. Implantation of these implants includes the use of right and left hand sling implantation tools that produce transvaginal, transobturator, suprapubic, or postpubic exposures or pathways. Also included is a delivery system that couples the end of the sling to the end of the elongated insertion tool and pulls the sling extension through the tissue pathway. The right hand and left hand insertion tool needles described in US Pat. No. 6,057,056, cited above, have bends in a single plane and are generally described in American Medical Systems, Inc. Corresponds to the BioArc® SP and SPARC® disposable sling implantation tools sold by the company in kits with elongated urethral slings.

  In some sling implantation kits, the needle portion comprises a proximal straight portion extending from the handle and a distal curved portion terminating at the end or tip of the needle. As described in the above-cited US Pat. No. 6,057,073, the kit includes one or more types of implantation tools (also referred to as “insertion tools”). The kit includes one tool suitable for outside-in surgery (eg, from skin incision to vaginal incision) and inside-out surgery (eg, from vaginal incision to skin incision). And another tool suitable for. Surgeons who prefer an approach determined by the surgeon's dominant hand can select the surgical and appropriate implantation tools. Alternatively, universal implantation tools (eg, right and left sling implantation tools, each suitable for both inside-out and outside-in methods) can be provided.

  Optionally, a removable protective sheath can wrap around the part of the pelvic implant extension. A connector (eg, an expansion connector) can be attached to the end of the extension to connect to one end of the insertion tool. Generally, the end of the insertion tool is inserted axially into the connector and the extension of the implant is pulled through the tissue path through the connector and needle to provide a central support for the pelvic tissue (eg, urethra). Pull and give support. The connector is pulled through the skin incision and the implant and sheath are cut in the vicinity of the connector.

  A similar transocclusive muscle transplantation procedure for transplanting a pelvic implant that restores and supports a pelvic organ, such as the vagina, to an appropriate anatomical position is assigned to the same assignee as the present applicant. And Patent Document 16. Generate a tissue pathway that exits the skin beside the anus and implants an implant that extends between the skin incisions to restore and support a pelvic organ, such as the vagina, to an appropriate anatomical location Another implant transplantation procedure is described in US Pat. Nos. 5,058,086 and 6,048,086, assigned to the same assignee as the present applicant. Various methods for attaching the sheath end and the mesh extension of the implant to the self-fixating tip are described in detail, for example, in the aforementioned US Pat. A further method of attaching an implant extension to an implantation tool is described in US Pat.

  This patent application describes pelvic implants and methods for treating pelvic illnesses, such as incontinence (stool incontinence, stress urinary incontinence, urge incontinence, mixed incontinence, etc.) ), Vaginal prolapse (including various forms such as intestinal, cystocele, rectal aneurysm, vaginal tip prolapse or vaginal prolapse, uterus drop), and other symptoms caused by muscle and ligament weakness is there.

  An embodiment of the implant includes a tissue support portion and one or more extension portions. Some implants include multiple elements. The elements of one embodiment are a support portion element that includes a tissue support portion and a support element arm that extends from the tissue support portion. An element of another embodiment is an extension part element that attaches to the support part element in an adjustable manner, for example with an accessory that includes a friction adjustment element for adjusting the length of the extension part. The multi-element structure and frictional adjustment element allows adjustment of the length of the extension, eg, the length measured from the distal end of the extension to the central support portion.

  The friction adjusting element is a connector or an adjustable element disposed on an extension or support part element, for example a tissue support part or an arm element of the support part. The friction adjusting element generally includes an opening and a frictional engagement that contacts the element of the implant material, the element of the implant material being, for example, an element of an elongated implant material that is threaded through the opening, Or an element of an extension from either a support part element (eg, an arm element of the support part). Embodiments of the friction adjustment element can allow unidirectional adjustments such as shortening the length of the extension. Other embodiments of friction adjustment elements include switching, actuating, removing, adjusting the length of the extension and locking or locking the friction adjustment element in a selected position to prevent movement in either direction. Can be adjusted in two directions: adjustment of the structure or mechanism of closing, or opening.

  Embodiments of the bi-directional friction adjustment element can include a guard or other structure that prevents contact between the friction surface of the connector and the implant element during bi-directional adjustment of the connector. The guard can be removed to engage the friction surface of the connector with the elements of the implant and prevent relative movement. Alternatively, the friction adjusting element allows the implant element to move freely in two directions through the opening, and a closed configuration that closes the friction surface against the implant element and prevents relative movement. And can be included. A user (eg, a surgeon) can manipulate the friction adjustment element between an open configuration and a closed configuration.

  The implant of the present invention can include a tissue fastener at the distal end of the extension. Tissue fasteners can be of various types, for example, self-fixating tips inserted into soft tissue and held by friction, other forms of soft tissue anchors, biological adhesives, and close to grip tissue This includes a soft tissue clamp, which typically has opposing jaws, and opposing male and female connector elements that engage and secure the ends of the extension to the tissue.

  The tissue fastener can be placed and secured within the internal tissue of the pelvic region and supports the implant and the pelvic tissue supported by the implant. As an example, tissue fasteners include obturator muscle tissue, tendon arch tissue, tissue in the tendon arch region, sacrospinous ligament tissue, tissue in the sacrospinous ligament region, coccyx region tissue, sciatic spine region Tissue, coccygeous muscle tissue, iliac coccygeous muscle tissue, uterine sacral ligament tissue, and levator tissue.

  In another embodiment of the implant and method, the distal end of the extension can be attached to the bone or can extend into the outer incision.

  Embodiments of tissue fasteners, such as self-fixating tips, are designed to engage the distal end of the insertion tool, and by pushing, the insertion tool can place the self-fixating tip at a desired tissue location. Designed as such.

  Implants can be implanted to treat pelvic disease by supporting pelvic tissue. According to a typical method, the physician identifies the tissue in the pelvic region to be supported and the tissue path through which the extension of the pelvic implant passes for support. The insertion tool and extension can be guided through the inner incision to insert the implant assembly. This surgery can be performed using a single (inner) incision by fixing the end of the extension to internal tissue (soft tissue, bone, fascia, etc.), or another embodiment Then, one or more extensions can be passed from the inner incision to the outer incision. One or more extensions of the implant are adjustable and can include frictional adjustment elements. The method can include adjusting the length of the one or more extensions and adjusting the position of the implant relative to the tissue to be supported, particularly the position of the tissue support, or adding to the tissue support by the extension. Adjusting the applied tension.

  An exemplary method of using an implant that includes a friction adjusting element can include implanting the implant by securing the distal end of the extension to tissue in the pelvic region. The central support portion can then be placed as desired and the length of the adjustable extension can be adjusted.

  Implants described herein include implants (eg, slings) that treat male or female urinary incontinence, where the slings include a tissue support portion and one or more (eg, two, four, etc.). , 6 or 8). The sling can comprise one or more of the features described herein, where the one or more features include an adjustment function that allows adjustment of the length of one or more extensions, a multi-layer or “hybrid” type A tissue support portion, a multi-element structure, and one or more tissue fasteners described herein, and can be combined with the insertion tools described herein.

  Similarly, other implants described herein, such as implants with two, four, or six legs that treat prolapse and male or female fecal incontinence, etc. are described herein. Can include a single feature or combination of features as described in the above, which includes an adjustment function that allows adjustment of the length of one or more extensions, a multi-layer or “hybrid” type tissue It includes a support portion, a multi-element structure, one or more tissue fasteners described herein, or in combination with an insertion tool described herein.

  The implants, methods, and insertion tools described herein allow pelvic floor reconstruction surgery to be performed with small incisions, making it easier to use various pelvic floor surgery groups. The implants described herein can be used to treat various areas of the pelvic floor, using tissue fasteners placed on several different anatomical landmarks to treat various areas of the pelvic floor There are anterior repair, posterior repair, tip support, perineal support (arrangement at the opening of the levator hiatus), fecal incontinence, and hysterectomy with a cap support. These markers are white lines, muscle and fascial layers, ligament structures (sacral ligaments, sacrotubular ligaments, proximal ligaments, circular cords, uterine sacral ligaments, perineal ligaments, and rectal ligaments) and the like.

  In one aspect, the invention relates to a multi-element pelvic implant that includes a tissue support portion and an extension portion. These elements include a support portion element having a tissue support portion and optional support portion element arms, and an extension portion element. The extension part element is adjustably connected to the support part element. The implant includes a friction adjustment element that allows adjustment of the length of the extension. The friction adjustment element includes an opening through which the element of the extension portion extends and a surface that frictionally engages the element of the extension portion. Friction engagement allows the extension element to move preferentially in one direction through the opening and prohibits movement of the extension element in the opposite direction.

  In another aspect, the invention relates to a multi-element pelvic implant that includes a tissue support portion and an extension portion. These elements include a support part element having a tissue support part and optional support part element arms, and an extension part element. The extension portion element is adjustably connected to the support portion element by a friction adjustment element that allows adjustment of the length of the extension portion. The friction adjustment element includes an opening through which the element of the extension portion extends and a surface that frictionally engages the element of the extension portion. The friction adjusting element has a first configuration that allows two-way movement of the element of the extension through the opening, and a surface frictionally engages the element of the extension, so that it passes through the opening in at least one direction. It is possible to have two configurations, a second configuration that prevents movement of the elements of the extended portion.

  In another aspect, the invention relates to a multi-element pelvic implant that includes a tissue support portion and an extension portion. These elements include a support part element comprising a tissue support part and optional support part element arms, and an extension part element. The extension part element is adjustably connected to the support part element by an elongate element of the extension part of the other of the two elements through the opening of one of the two elements. A friction adjustment element is arranged on the elongated element of the extension part so that the length of the extension part can be adjusted. The friction adjustment element includes an opening through which the elongated element of the extension portion extends and a surface that frictionally engages the element of the extension portion. Friction engagement preferentially allows movement of the elements of the extension through the opening in one direction and prohibits movement of the elements of the extension in the opposite direction.

  In another aspect, the invention relates to a surgical implant for treating a pelvic disease. The implant includes a tissue support portion and an extension portion. The tissue support portion includes a plurality of layers of material including a layer of synthetic material and a layer of biological material.

  In another aspect, the invention relates to a surgical implant for treating pelvic disease. The implant includes a tissue support portion, an extension portion, and a tissue clamp at a distal end of the extension portion.

  In another aspect, the invention relates to a surgical implant for treating pelvic disease. The implant includes a tissue support portion, an extension portion, and a tissue fastener at the distal end of the extension portion. The tissue fastener includes a male engagement element and a female engagement element.

  In another aspect, the present invention relates to a surgical implant and a combination of tools useful for installing the surgical implant. The surgical implant includes a support portion, an extension portion, and a self-fixating tip at the distal end of the extension portion. The tool includes a finger sack that can be placed on a finger and a distal end that engages a self-fixating tip.

  In another aspect, the present invention relates to a surgical implant and a combination of tools useful for installing the surgical implant. The surgical implant includes a support portion, an extension portion, and a self-fixating tip at the distal end of the extension portion. The tool includes a handle and an elongated curved shaft with a proximal end and a distal end. The proximal end is connected to the handle and the distal end is connected to the end element through the bend. The elongated curved shaft has a length in the range of 6-12 inches (152.4-304.8 mm). The angle between the tangents at the ends of the curved shaft is in the range of 120-150 degrees. The bent portion has an angle within a range of 120 to 150 degrees. The end elements have a length of about 0.25 to 1 inch. The end element has a distal end that engages a self-fixating tip.

  In another aspect, the present invention relates to a surgical implant and a combination of tools useful for installing the surgical implant. The surgical implant includes a support portion, an extension portion, and a self-fixating tip at the distal end of the extension portion. The tool includes a handle and an elongate shaft, the elongate shaft comprising a proximal end connected to the handle and a distal end connected to the pivoting loop portion. The loop portion includes a distal end that engages a self-fixating tip.

  Another aspect of the invention relates to a surgical tool useful for implanting pelvic implants. The tool includes a handle, a cannula connected to the handle, and a shape memory wire slidably disposed within the cannula. The shape memory wire has a natural shape that is different from the shape of the cannula.

  Another aspect of the invention relates to a method of treating a pelvic disease. The method includes generating an inner incision, providing a pelvic implant as described herein, an insertion tool as described herein, or a combination of an implant and a tool, and passing the implant through the incision. And placing the implant at a desired support location in relation to the tissue of the pelvic region.

  Another aspect of the invention relates to a method of treating a pelvic disease. The method includes providing a pelvic implant as described herein, an insertion tool as described herein, or a combination of an implant and a tool, and adjusting the distal end of the adjustable extension to tissue in the pelvic region. And adjusting the length of the adjustable extension.

  Other features and advantages of the present invention will become apparent by reference to the following description of specific embodiments in connection with the accompanying drawings. The accompanying drawings are schematic and therefore are not to scale.

FIG. 6 shows a plan view of a pelvic implant having two legs. FIG. 6 shows a plan view of a pelvic implant having four legs. FIG. 6 shows a plan view of a pelvic implant having six legs. Fig. 2 shows a perspective view of a multi-element implant according to the invention. Fig. 3 shows a plan view of the implant of Fig. 2; 1 shows an embodiment of a friction adjusting element according to the invention. 1 shows an embodiment of a friction adjusting element according to the invention. FIG. 5 shows a cross-sectional view of the friction adjustment element of FIGS. 3 and 4. Fig. 4 shows a cross-sectional view of another embodiment of a friction adjusting element according to the invention. Figure 2 shows an exploded view of one embodiment of a friction adjustment element comprising a guard according to the present invention. 1 illustrates one embodiment of an adjustable pelvic implant according to the present invention. 1 shows a multi-element implant or part of a multi-element implant comprising a friction adjusting element according to the invention. 10 shows a sheath of a portion of the implant of FIG. 1 shows a multi-element implant and adjustment tool according to the present invention. 1 illustrates an exemplary multi-element pelvic implant according to the present invention. 1 illustrates an exemplary multi-element pelvic implant according to the present invention. 1 shows a multi-element implant and adjustment tool according to the present invention. 2 shows an example of an exemplary adjustment tool according to the present invention. 2 shows an example of an exemplary adjustment tool according to the present invention. 1 shows a multi-element implant and adjustment tool according to the present invention. Fig. 4 shows an embodiment of means for attaching a friction adjusting element to an implant according to the invention. Fig. 4 shows an embodiment of means for attaching a friction adjusting element to an implant according to the invention. Fig. 4 shows an embodiment of means for attaching a friction adjusting element to an implant according to the invention. Fig. 4 shows an embodiment of means for attaching a friction adjusting element to an implant according to the invention. Fig. 4 shows an embodiment of means for attaching a friction adjusting element to an implant according to the invention. Fig. 4 shows an embodiment of means for attaching a friction adjusting element to an implant according to the invention. Fig. 4 shows an embodiment of means for attaching a friction adjusting element to an implant according to the invention. 2 illustrates an embodiment of a multi-layer or hybrid pelvic implant according to the present invention. 2 illustrates an embodiment of a multi-layer or hybrid pelvic implant according to the present invention. 2 illustrates an embodiment of a multi-layer or hybrid pelvic implant according to the present invention. Figure 3 shows an insertion tool for placing an implant according to the present invention. Figure 3 shows an insertion tool for placing an implant according to the present invention. 27 shows the insertion tool of FIGS. 25-26 when used with a pelvic implant. FIG. Figure 3 shows an insertion tool for placing an implant according to the present invention. Fig. 4 shows an embodiment of an insertion tool for placing an implant. Fig. 4 shows an embodiment of an insertion tool for placing an implant. Fig. 4 shows an embodiment of an insertion tool for placing an implant. Fig. 4 shows an embodiment of an insertion tool for placing an implant. Fig. 6 shows an implant with an extension disposed around a tendon arch. Fig. 6 shows an insertion tool for placing an implant around a tendon arch according to the present invention. Fig. 6 shows an insertion tool for placing an implant around a tendon arch according to the present invention. Fig. 6 shows an insertion tool for placing an implant around a tendon arch according to the present invention. Fig. 6 shows an insertion tool for placing an implant around a tendon arch according to the present invention. Figure 3 shows another insertion tool for placing an implant. Figure 3 shows another insertion tool for placing an implant. Fig. 2 shows a tissue clamp according to the invention in an open or unlocked shape. FIG. 40 shows the tissue clamp of FIG. 39 in a closed or locked configuration. FIG. 40 shows a schematic view from above of the open shape of the tissue clamp of FIG. 39; FIG. 41 shows a schematic view from above of the closed shape of the tissue clamp of FIG. 40; Fig. 3 shows an extension that can be used for a pelvic implant according to the present invention. 1 shows an exemplary implant according to the present invention. 1 shows an exemplary implant according to the present invention. 44 shows an insertion tool for installing the implant shown in FIGS. 44 and 44A. FIG. 45 shows the implant of FIG. 44 implanted in tissue. 1 illustrates an exemplary tissue fastener and associated insertion tool according to the present invention. 1 illustrates an exemplary tissue fastener and associated insertion tool according to the present invention. 1 illustrates an exemplary tissue fastener and associated insertion tool according to the present invention. 1 illustrates an exemplary tissue fastener and associated insertion tool according to the present invention.

  The following description is for illustrative purposes only and is not intended to be limiting. In view of this description, other embodiments of the invention will be apparent to those skilled in the art.

  The present invention relates to surgical instruments, assemblies, and implantable articles for treating pelvic floor disorders such as fecal or urinary incontinence including stress urinary incontinence (SUI) and prolapse. According to various embodiments, surgical implants can be used to treat pelvic disease, such as surgical placement of surgical implants to remove vaginal foramen or incontinence (male or female), etc. Specific examples of treating the condition are included. Various features of surgical implants, surgical tools useful for installing implants, surgical systems, surgical kits, and surgical methods are described. Implanting an implant into a man or woman and urgent incontinence, stress urinary incontinence, mixed incontinence, overflow incontinence, functional incontinence, fecal incontinence, or female disease, prolapse (eg, vaginal or uterine) ), Intestinal (eg, uterine), rectal, cystocele, and anatomical hypermotility, or diseases involving combinations of two or more thereof, and the like.

  The implant includes a tissue support portion that is used to support pelvic tissue such as the urethra (including the bladder neck) and vaginal tissue. In use, the tissue support portion is typically placed in contact with the tissue to be supported and attached thereto, such as with a suture. The implant can further include one or more extensions attached to the tissue support portion. Optionally, a tissue fastener can be included at one end of the extension portion, the tissue fastener being designed to be attached to tissue within the pelvic region to secure the distal end of the extension portion to the tissue.

  The tissue support portion is designed to support a particular type of pelvic tissue such as the urethra, bladder, or vaginal tissue (such as anterior, posterior, tip). The tissue support portion, when installed, can be sized and shaped to contact the desired tissue, for example, a “sling” or “hammock” that contacts and supports the pelvic tissue. The size is set and molded. As used herein, tissue support portions disposed between a plurality of extensions are often referred to as “central support portions” or “support portions”.

  The extension portion is an elongated piece of material that extends from the tissue support portion and is useful for providing support for the tissue support portion and the supported tissue by passing through or attaching to tissue in the pelvic region. is there. One or more (eg, one, two, four, or six) extensions extend from the tissue support portion, eg, extend through the tissue pathway to an internal anchor point (such as a bone anchor or tissue fastener) Can be attached to tissue in the pelvic region by extending to the outer incision.

  A typical implant can be manufactured from a material according to a conventional implant and shaped and sized according to a conventional implant, but it is here described as a friction adjustment element, a multi-element structure, a multi-layer tissue support portion, etc. Changes can be made to include the described features. For example, an implant is disclosed in Patent Document 20 filed on April 30, 2004, Patent Document 21 filed on November 27, 2002, Patent Document 22 filed on February 3, 2006, Patent Document 23 filed on February 3, 2006, Patent Document 24 filed on February 3, 2006, Patent Document 25 filed on February 3, 2006, February 3, 2006 Patent Document 26 filed on date, Patent Document 27 filed on April 5, 2005, Patent Document 28 filed on October 5, 2005, and filed on May 7, 2004 Patent Literature 29, and Patent Literature 30 with the national filing date of July 25, 2006, can be provided with the features described in the typical literature, each of which is incorporated herein by reference. Yo It is encompassed herein.

  Typical implants are for the treatment of pelvic prolapse (including vaginal vault prolapse, cystocele, intestinal aneurysm, etc.) under the registered names Apogee® and Perigee®, and for urinary incontinence For treatment, American Medical Systems, Inc., Minnetonka, Minnesota, under the registered trade names Sparc®, Bioarc®, and Monarc®. Can be made from materials similar to those commercially available from and can have similar approximate sizes and shapes.

  The implant can include portions or sections of synthetic material or biological material (eg, pigs or human cadaver). The extension (manufactured from a single piece or multiple pieces) can be, for example, a synthetic mesh such as a polypropylene mesh. The tissue support portion can be a synthetic material (eg, a polypropylene mesh) or a biological material.

  Commonly useful, typical implant types described herein may include those conventionally or currently used for the treatment of pelvic illnesses, among the terms for pelvic implants: Implants called urethral “slings”, “strips”, “mesh strips”, “hammocks” can be included. For example, an example of an implant for treating incontinence such as a urethral sling can include a central support portion and two extension portions. A typical urethral sling can generally be in the form of an implantable strip having a support portion comprised of a central support portion and two extensions. An example of a urethral sling for treating male urinary incontinence comprises a wide central support, as described in, for example, co-pending US Pat. be able to. Other exemplary urethral sling implants are described, for example, in co-pending US Pat.

  Examples of implants for treating vaginal prolapse can include a central support portion and two, four, or six extensions, and can be a multi-piece mounted in an integral mesh or modular fashion. It can take the form of a mesh. For example, see Patent Document 31, Patent Document 20, Patent Document 28, Patent Document 29, and Patent Document 30, which are co-pending with the assignee of the present application.

  The dimensions of the implant can be desirable and useful for any particular placement procedure, treatment, patient structure, to support a particular tissue or tissue type. A typical dimension is that the tissue support portion is brought into contact with the tissue to be supported and the extension portion extends from the tissue support portion to a desired anatomical location, and the extension portion is secured to tissue in the pelvic region. Be sufficient to pass through and support the tissue support.

  The dimensions of the extension according to the present invention support the pelvic tissue (at the "proximal end side" end of the extension connected to the tissue support part), as required, according to various installation procedures. The extension portion can be extended between the tissue support portion disposed therefor and the location where the distal end of the extension portion attaches to the pelvic tissue or passes through the outer incision.

  The distal end of the extension according to embodiments of the present invention can include a tissue fastener that is attached to tissue in the pelvic region. Tissue fasteners can be, for example, soft tissue anchors, self-fixating tips, biological adhesives, tissue clamps, opposing male and female connector elements that engage tightly when pressed against each other, or the distal end of an extension It can be any other device that secures the part to the tissue in the pelvic region. The implant is also designed, for example, for the distal end to be secured to the tissue by other methods (eg, sutures) or to pass through the outer incision. In some cases, the distal portion of the extension may include an extension that does not include a tissue fastener.

  The distal end of the extension can be attached to any desired tissue in the pelvic region, or can reach the outer incision through the desired tissue path. To attach the extension to the tissue, a tissue fastener can be attached to the distal end of the extension. When installing an implant, the tissue fastener is, for example, a fibrous tissue such as a muscle (eg, obturator, internal obturator, external obturator, levator ani, coccyx, iliac coccygeus), sacrospinous ligament, etc. Can be attached to a desired tissue such as a ligament or surrounding tissue, a tendon or surrounding tissue such as a tendon arch, or a sciatic spine or nearby tissue.

  By way of example, the extension is published as of February 8, 2007 and is described in Applicant's co-pending US Pat. No. 5,834,049 entitled “Methods and Symptoms for Treatment of Prolapse”. It can be attached to the tissue of the arch or to the tissue in the area of the tendon arch, the entire contents of which are hereby incorporated by reference. A typical pelvic implant is used to provide structural support and treat vaginal prolapse (eg, vaginal prolapse, intestinal aneurysm, and rectal aneurysm) as described in US Pat. be able to. The implant passes through a tissue support portion attached to the vaginal tissue and optionally from the posterior vaginal tissue to a location in the area of the tendon arch ("white line"), optionally in the vicinity of the sciatic spine, eg, 1 cm from the sciatic spine. One or more extensions (eg, two extensions). The implant may be, for example, at the level of the sciatic spine at the level of the sciatic spine in the vicinity of the connection of the sciatic spine to the tendon arch, through a tissue pathway including a passage through the tissue at the immediate anterior edge of the sciatic spine, from the vaginal tissue attachment point. You can pass up or down.

  The extension portion is extendable through a tissue pathway that terminates in a tendon arch, and includes, for example, a tissue fastener that secures the distal end of the extension portion to the tendon arch. Alternatively, the tissue path can wrap around the outer part of the tendon arch (relative to the area of the pelvic floor), so that the extension of the implant is in the vicinity of the tendon arch (above or above the tendon arch). A tendon arch that exits the pelvic region (downward) and continues along a path that wraps or bends around the white line and then (optionally) is on the other side of the white line, i.e., opposite the entry direction Means re-entering the pelvic region either below or above. The tissue path can include a relatively sharp turning radius to place the extension in the vicinity of the tendon arch. By extending around the white line, the extension can come into contact with the tissue surrounding the white line and, as a result, become engulfed into the tissue. This internal biting can provide fixation of the extension into the tissue.

  A preferred example of a tendon arch region can be formed as a curved rectangular shaped region that extends 2 cm above and 2 cm below the tendon arch (eg, 1 cm above and 1 cm below) and begins with a sciatic spine For example, it is configured to include a region having a length extending in the anterior direction along the tendon arch at a distance of about 3 cm forward of the sciatic spine (eg, about 1 cm forward of the sciatic spine). A particularly preferred tissue path is very close to or as close as possible to the sciatic spine, and may be above or below the tendon arch, for example at the immediate anterior edge of the sciatic spine, near the connection of the sciatic spine to the tendon arch. It passes through the tissue at the level of the sciatic spine and the dimensions are 0.5 or 1 cm above or below the tendon arch and can be 0.5 or 1 cm anterior to the sciatic spine along the tendon arch.

  Another example of a location for attaching the end of the extension is through the coccyx region, as described in Applicant's co-pending US Pat. And the content of US Pat. No. 6,057,086 is hereby incorporated by reference in its entirety. The patent application 27 application describes the use of implants to treat vaginal prolapse (eg, vaginal fornix prolapse, intestinal aneurysm, cystocele, rectal aneurysm) using an implant comprising a tissue support portion and an extension portion. In this case, the extension passes through a tissue pathway that includes the region of the coccyx (ie, the “coccyx region” or “transcoccusal” tissue pathway).

  Exemplary methods of the present invention include the placement of support members to support the prolapsed tissue, for example, attached to muscles (sciatic and iliac coccyges) or lateral ligaments (sacral spinal ligaments) Including placement of an extension portion of a support member in the coccyx region proximate to the coccyx, such as or made through or through. A typical tissue pathway can start from the area surrounding the vaginal cavity tissue and can extend past the rectum to a location close to the coccyx. The extension of the support member can generally be guided through a passage provided in the muscle or other tissue attached to the tissue internally in this region, past the rectum and in proximity to the tailbone. The distal end of the extension can be attached to any tissue in the coccyx region, such as by a tissue fastener that secures the distal end of the extension to a muscle or ligament (eg, sacrospinous ligament) in the coccyx region. . Alternatively, the distal end of the extension can extend through the tissue in the coccyx region toward the outer incision in the epidermis.

  A typical coccyx region generally extends from the tip of the coccyx along the side edge of the coccyx, continues along the lower side edge of the sacrum, extends toward the upper edge of the sacrospinous ligament 202, and then Crossing toward the sciatic spine, the lower boundary extends between the sciatic spines, extends along a folded path that includes a point about 2.5 cm lateral to the tip of the coccyx and returns to the apex of the coccyx. The extension can be attached to tissue in this region or can pass through tissue in this region to the outer incision.

  Another typical coccyx region can be bounded by an edge of the coccyx, the lower edge of the sacrospinous ligament towards the sciatic spine, a point approximately 2.5 cm lateral to the apex of the coccyx, and the apex of the coccyx. The extension can be attached to tissue in this region, or can pass through tissue in this region toward the outer incision.

  Yet another embodiment of the coccyx region is generally a coccyx, for example, up to about 2.5 cm lateral to the inclined vertical edge of the coccyx toward the upper horizontal edge of the coccyx adjacent to the sacrum from the tail tip of the coccyx. By the vertical edge of the tailbone between the tip of the bottom coccyx and the lower edge of the sacrum, and a 2.5 cm line laterally parallel to this edge from this edge This is the area where the boundary is defined. The extension can be attached to tissue in this region, or can pass through tissue in this region toward the outer incision.

  Another example of where to attach one end of the extension is in a tissue path that passes through or terminates in the region of the sciatic spine. The tissue in the region of the sciatic spine can be tissue within 1 cm of the sciatic spine, including the levator ani (iliac coccygeus) and tendon arch tissue. The distal end of the extension can be attached to tissue in this region, such as with a soft tissue fastener. The tissue in this area can be relatively thin compared to other tissues in the pelvic area, which allows the tissue fasteners to be firmly attached to this relatively thin tissue. It means that it can be adapted. One example of a tissue fastener that is particularly useful for attaching to tissue in the region of the sciatic spine is the tissue clamp described herein.

  In another embodiment, the tissue pathway can pass in the region of the sciatic spine, in the vicinity of the sciatic spine, and then towards other structures such as the lateral incision in the rectum or perirectal region. An example of such an organization route is described in the applicant's co-pending Patent Document 20 filed on April 5, 2006, the contents of which are all incorporated herein by reference. Are encompassed herein. The application of U.S. Pat. No. 6,057,031 describes implants and methods useful for the treatment of vaginal prolapse, vaginal prolapse, intestinal aneurysm, rectal aneurysm, etc., from the prolapsed organ to the area of the sciatic spine, and , Including the tissue path towards the outer incision. The tissue pathway can pass through the levator muscle in the vicinity of the sciatic spine.

  Still other examples of tissue pathways for supporting the posterior tissue of the vagina by an extension are described in the applicant's co-pending US Pat. Is incorporated herein by reference in its entirety. Such a tissue path is directed to the sacrum (and attached internally to the sacrum) or to an external incision in the perirectal region (eg, through the region of the sciatic spine). Can be.

  Useful tissue pathways and structures for an extended portion of an implant that supports anterior vaginal tissue, bladder, bladder neck, urethra, or combinations thereof are described in commonly assigned US Pat. The tissue pathways described in document 21 can be included, the contents of these patent documents are hereby incorporated by reference in their entirety. Such tissue pathways can go to the obturator foramen, pubic bone, rectus fascia, retropubic space (internally attached), through the obturator for an external incision in the thigh region, or straight It can be directed through the fascia to the outer incision in the abdomen.

  As described elsewhere herein, the length of the extension (extending through any tissue pathway) can optionally be fixed or adjustable. This allows the surgeon to change the length of the extension before, during, or after implantation. On the other hand, adjustment and from an embodiment of the implant or from a specific extension such as, for example, an upper extension or an extension located in a tissue path extending towards the outer incision that will be attached to the closure hole. It is also possible to exclude the tension mechanism.

  An example of an implant for use as described herein is an implant having one or two legs useful for treating posterior vaginal prolapse, such as vaginal fornix prolapse, intestinal aneurysm, rectal aneurysm, and the like. can do. Such an implant is shown in FIG. The implant 40 includes a central support portion 42 and one or more extension portions 44. The extension may optionally and preferably adjust the distance between the distal end of the extension and the fixed position of the tissue support portion to allow adjustment of the length of one or two extensions. Or a shortening adjustment function (not shown). As shown, the extension portion 44 has an angle (a) with respect to the longitudinal axis 46 of the central support portion 42, which is the tissue support when the implant is placed flat. As measured between the line 46 formed by the longitudinal axis of the portion 42 and the longitudinal axis 48 of the end portion 44, it is in the range of 30-60 degrees, for example 35-55 degrees or 40 ~ 50 degrees.

  Still referring to FIG. 1, the support portion 42 is shown as being constructed from a mesh, but instead, from a non-mesh (eg, biological) material or from a non-mesh biological layer. And a plurality of layers including a synthetic mesh layer. Each extension 44 can optionally include a tissue fastener (not shown) attached to the distal end of each extension 44. Such implants are available from American Medical Systems, Inc. It can be similar to the Apogee (registered trademark) product product commercially available from the company. The distal end of the extension may be applied to the internal tissue in the area of the sciatic spine, to muscle tissue such as the coccyx, iliac coccyx, or levator ani, as desired, for example by using a tissue fastener. It can be placed in tissue in the tendon arch region (including tendon arch), in the coccyx region, in the sacrospinous ligament tissue, in the uterine sacral ligament tissue, in the sacrum (bone), and the like. Alternatively, the distal end can pass either of these tissues towards the outer incision.

  Another embodiment of the implant is an implant having four legs useful for treating anterior vaginal prolapse and optionally urinary incontinence. An example of such an implant is shown in FIG. 1A. Implant 50 includes a central support portion 52 and four extensions, two upper extensions 54 and two lower extensions 56. Two or four of the extensions 54 or 56 can include a frictional adjustment element (not shown), or none of the extensions can include it. The upper extension 54 may be a fixed length or may include a friction adjustment element.

  With further reference to FIG. 1A, the support portion 52 is shown as being composed of a mesh, but instead, from a non-mesh (eg, biological) material or a non-mesh biological layer. And a plurality of layers including a synthetic mesh layer. Each of the extensions 54 and 56 can optionally include a tissue fastener (not shown) attached to the distal end of each extension. Such implants are available from American Medical Systems, Inc. It can be similar to the Perigee® product product commercially available from the company. The tissue fastener at the end of the lower extension 56 includes, as desired, in the area of the sciatic spine, in the sacrospinous ligament (eg, within 1 cm of the sciatic spine), and in the area of the tendon arch (including that of the tendon arch). ) Can be placed in the tissue of the obturator (eg, internal obturator muscle). The distal end of the upper extension 54 can be attached to the obturator, as desired, or passed through the obturator towards the lateral incision, retropubic space, abdominal incision, rectus fascia, etc. , Can be arranged laterally towards the closure hole.

  Optionally, the four-legged implant 50 includes one or more additional extensions and constitutes an six-legged implant that is useful for treating prolapse, such as anterior prolapse, for example. You can also. A typical six leg implant is shown in FIG. 1B. The implant 60 includes, for example, two upper extensions 64 that can be secured to the obturator or alternatively can pass through the obturator toward the outer incision in the internal thigh, and tissue in the coccyx region (eg, sacral). Two lower extensions 62 for placement in the tissue of the coccyx region, for example, by internal fixation to the spinal ligament) or by passing the tissue of the coccyx region towards the lateral incision 4 Includes two extensions. The implant 60 can be secured to internal tissue (eg, in the area of the sciatic spine (eg, the levator ani or tendon arch)) or passed through the area of the sciatic spine toward the lateral incision. Two additional extensions 66 that can be secured to the tissue of the desired pelvic region, such as the area of the tendon, the area of the tendon arch, or the obturator.

  Any of the implants of FIGS. 1, 1A, or 1B, or any variation thereof, can include one or more additional extensions, for example for attachment to a sacrum or uterine sacral ligament.

  In accordance with various embodiments of the implant described herein, the implant includes a friction adjustment element to allow adjustment of the length of the extension and to adjust the position or tension of the implant. Multiple elements may be included that are adjustably connected to one by one. By “multi-element” implant is meant an implant comprising a “supporting partial element” and one or more “extending partial elements”. The “support subelement” is connected to the “extension subelement” by an element that includes a “friction adjustment element” that can be used to adjust the length of the extension. The support portion element includes a tissue support portion and may optionally include one or more “support portion element arms” extending from the tissue support portion. The extension part element connects to the support part element, for example, at a tissue support part or at a support part element arm extending from the tissue support part of the support part element.

  According to one general embodiment of a multi-element implant, the support portion element includes a tissue support portion and one or more “support portion element arms” that extend from the tissue support portion and connect to the extension portion element. The support part element arm is an elongated extension of the support part element generally manufactured from a synthetic material that connects to the extension part element in a manner that allows adjustment of the length of the extension part composed of the support part element and the extension part element. can do. The “extension portion” of the implant is the one that collectively includes the extension portion elements and the support portion element arms. For example, see FIGS. 2 and 2A.

  According to another embodiment of the multi-element implant, the support part element is identical to the tissue support part. The support portion element includes a location for the elongated extension portion element to be adjustably connected to the support portion element. For example, see FIG. 10A.

  The frictional adjustment element can be secured to the implant at the tissue support portion or at a position along the length of the extension portion (which can be part of the extension portion element or the support portion element arm). (I.e., it is fixedly and immovably mounted rather than movably engaged). When fixed relative to the extension, the friction adjustment element can preferably be fixed to the distal end of the support part element arm or to the proximal end of the extension part element. For example, an implant element, such as an elongate element of the extension (which can be part of the extension part element or part of the support part element arm) passes through the opening of the friction adjustment element or other You can pass this in the way. The frictional adjustment element is frictionally engaged with the implant element, for example, by a friction surface, such as a tooth, jaw, or other opposing frictional surface, in one or two directions between the friction adjustment element and the implant element. Relative movement can be allowed or relative movement in one or two directions can be prevented.

  Certain exemplary implants according to the present invention include a tissue support portion that includes multiple layers of one layer made from a biological material and one layer made from a synthetic material such as a polymer mesh. be able to. The multiple layers optionally have the same size and shape, similar size and shape, or different sizes and shapes.

  The multi-layer tissue support portion can include a biological layer sized and shaped to contact the tissue to be supported (eg, vaginal tissue), and two layers of tissue having the same extent To generate the support portion, a synthetic layer having the same size and shape as the biological layer can be provided. In this embodiment, the tissue support portion can include a synthetic mesh layer and a biological layer that are, for example, identical or substantially identical in shape and size, the mesh layer being beyond the area of the biological layer. One or more support part element arms may be further included.

  The two layers of the multi-layer tissue support portion can be formed and held together as desired by stitching, stitching, stapling, bonding, thermoforming, polymeric rivets, and the like. When used, the biological layer can be placed adjacent to sensitive tissue such as, for example, vaginal tissue to prevent tissue wrinkling.

  In another embodiment, the biological layer can be sized and shaped to support and support tissue, the synthetic layer extending between the sides, for example across the width of the tissue support portion, It may have a relatively small area (see FIGS. 23 and 24) arranged to reinforce the tissue support portion at that location. The synthetic mesh layer may be in the form of a “band” or “strip” of material that extends across the width of the tissue support portion. The length of the composite strip may be the same as the width of the tissue support portion or may exceed the width of the tissue support portion, in which case the extending end of the composite strip is, for example, An extension or partial extension can be formed, such as a support part element arm that can be attached to the extension part element.

  An example of a particular type of pelvic implant is a type that includes or consists of a central support portion and two, four, or six elongated extensions extending from the central support portion. Implants with two extensions are of a type useful for the treatment of, for example, urinary incontinence, anterior vaginal prolapse, posterior vaginal prolapse, and implants with four or six extensions treat these combinations of conditions Would be useful to do. The term “supporting portion” refers to the portion of the implant that functions to support the tissue after the implantation of the implant is complete, specifically an extension portion (including frictional adjustment elements and tissue fasteners) and A tissue support portion, and does not include any or additional features of the implant, such as a sheath or other type of connector for attaching the implant to an insertion tool.

  The extension portion of the implant can include tissue fasteners at the distal end, such as tissue anchors, self-fixating tips, biological adhesives, tissue clamps, pairs of opposing male and female connector elements.

  A “self-fixating tip” is generally connected to the distal end of an extension that can be implanted in tissue in a manner that will maintain the position of the self-fixating tip and support the mounted implant. It can be a structure. Also, a typical self-fixating tip can be used at one end of the insertion tool (e.g., elongate needle or tube) so that the insertion tool can be used to push the self-fixating tip into tissue for implantation. It can also be designed to engage. The self-fixating tip can engage the insertion tool at an internal channel of the self-fixating tip, at an external location such as a base, or at a lateral extension, as desired.

  The self-fixating tip is generally made of any useful material, including materials that can be molded or formed into the desired structure and that can be connected or attached to one end of the implant extension. Useful materials include plastics such as polyethylene, polypropylene, and other thermoplastic or thermoset materials, and metals, ceramics, and other types of biocompatible and optionally bioabsorbable or bioresorbable. Absorbent materials can be included. Typical bioabsorbable materials include, for example, polyglycolic acid (PGA), polylactide (PLA), copolymers of PGA and PLA.

  The self-fixating tip can be inserted into tissue in the pelvic region and can then be in any form that will be retained in the tissue. A typical self-fixating tip is one or more lateral directions that can increase the force required to remove the self-fixating tip from the tissue after insertion into the tissue, i.e., "drawing force". Can include extensions. At the same time, the lateral extension can be designed to have a reduced or relatively small “insertion force” that is the amount of force used to insert the self-fixating tip into the tissue. . Self-fixating tips are designed to be essentially permanently positioned when inserted into tissue, with the exception of providing the desired placement of self-fixing tips or mounted implants If absolutely necessary to do so, the surgeon can remove the self-fixating tip in an implantation procedure. The self-fixating tip and all components of the self-fixating tip can be of combined form and size to result in these functional features. See U.S. Pat. No. 6,057,034, filed Feb. 16, 2007, entitled “Surgical Articles and Methods for Training Pelvic Conditions”. The entire contents of Patent Document 34 are hereby incorporated by reference.

  According to an exemplary embodiment, the self-fixating tip can comprise a structure including a base with a proximal end-side base end and a distal base end. The base end on the proximal end side can be connected to the distal end of the extension (directly or indirectly, such as by connecting sutures). The base extends from the base end on the proximal end side to the distal base end, and optionally distally at least partially along the length of the base from the base end on the proximal end side An internal channel extending toward the base end of the substrate. Any internal channel should be designed to interact (ie, engage) with the distal end of the insertion tool so that the insertion tool can be used to place the self-fixating tip at a location within the patient's pelvic tissue. Can do.

  Another embodiment of the self-fixating tip does not require an internal channel to engage the insertion tool and can be omitted. These alternative embodiments may be non-hollow without an internal channel and, for example, can be configured with a base (on the side or face of the base end on the proximal end side) as required. The insertion tool can be engaged by any form of engagement, such as by using an insertion tool that contacts the self-fixating tip at an external location, such as gripping or contacting a lateral extension.

  Also, self-fixating tip embodiments may be from a location between the proximal and distal ends, from a distal base end location, or from a proximal end side base end location, etc. As well as one or more lateral extensions extending laterally (eg, radially) from the base.

  The self-fixating tip can be connected to the extension of the implant directly by an attachment mechanism or indirectly through an attachment structure such as a suture. As described in Patent Document 35, the connection is based on a mechanical structure, by adhesion, by connection stitching, injection molding or “insert” molding (also “overmolding”), etc. The content of Patent Document 35 is incorporated herein by reference. According to this description, at one end of the mesh extension of the implant, the thermoplastic or thermosetting polymer material can be insert molded or injection molded directly into the mesh, for example. By this method, the molded polymer can form a self-fixating tip at one end of the extended portion. The self-fixating tip can be as described herein and includes, for example, a lateral extension and an internal channel.

  An insertion tool can be used to place the implant. Various types of insertion tools are known, and these types of tools and variations thereof can be used in accordance with the present specification to install an implant. Examples of useful tools include an elongated shaft attached to a handle, a handle attached to one end (proximal end) of the shaft, and an end of an extension such as, for example, a self-fixating tip. Includes tools of the type that generally include any distal end (or “end”) of the adapted shaft. The needle can facilitate placement of the distal end of the extension portion of the desired anatomical location, this structural location being internal or the tissue path towards the outer incision. Can be passed.

  Typical insertion tools for treating incontinence and vaginal prolapse are described in, for example, Patent Document 20, Patent Document 21, Patent Document 24, Patent Document 27, Patent Document 29, Patent Document 30, and Patent Document 35. The contents of each of these patent documents are incorporated herein by reference. The tools described in these patent documents are designed to place implants in the pelvic region for treatment such as prolapse and male or female incontinence. The tool is bendable in two or three dimensions, e.g., extending the implant through a tissue pathway that passes from the region of the urethra, through the obturator hole, toward the outer incision in the groin or internal femoral region. It can include a three-dimensional spiral portion for positioning the portion. Other insertion tools described include a two-dimensional elongate needle that allows the user to place an extension of the implant through the lower incision and the outer incision around the rectum or in the coccyx region.

  A typical insertion tool can be similar to the tools described in the above-cited patent literature or can include these features. By changing these insertion tools for use in accordance with the particular methods described herein, for example, using the insertion tool, the pelvis through a tissue pathway that does not extend toward the outer incision. A self-fixating tip can be placed on the tissue within the region. The insertion tool can be straight or curved in two or three dimensions and can be inserted through a vaginal incision (for a female structure) or a perineal incision (for a male structure) and extended It can be designed, shaped, and sized to include an elongate shaft that extends from the incision toward or through the pelvic tissue to place the distal end of the portion.

  FIG. 2 shows a typical multi-element implant 500. In FIG. 2A, the implant 500 is shown as an exploded view. The implant 500 includes a support portion element 501, a first extension portion element 504, and a second extension portion element 506. Support portion element 501 includes a tissue support portion 502 and first and second support portion element arms 508 and 510. First extension element 504 includes a frictional adjustment element 512 secured to the proximal end and a tissue fastener (eg, self-fixating tip) 514 at the distal end. Similarly, the second extension element 506 includes a frictional adjustment element 512 secured to the proximal end and a tissue fastener (eg, self-fixating tip) 514 at the distal end. Support portion element arm 508 and extension portion element 504 are combined to produce extension portion 505. Support portion element arm 510 and extension portion element 506 are combined to produce extension portion 503.

  According to some implant embodiments, the friction adjustment element may prevent the adjustment connector from contacting sensitive tissue (eg, vaginal tissue) supported by the tissue support portion when installed. The extension part element can be arranged at a position between the support part element arm and the extension part element. In certain implant embodiments, the frictional adjustment element can be positioned closer to the distal end of the extension portion than the tissue support portion of the implant, e.g., an extension between the friction adjustment element and the self-fixating tip. The length of the portion can be in the range of about 0.5 cm to about 1.0 cm.

  Referring to FIGS. 3, 4, and 5, the friction adjustment element 512 is shown in more detail. 3 shows a perspective view seen from above, FIG. 4 shows a perspective view seen from the bottom, and FIG. 5 shows a cross-sectional view. The friction adjustment element 512 includes a body 516, an opening 518, and a plurality of teeth 520. The opening 518 receives an element of the implant, such as, for example, a support partial element arm (508 or 510). When the support part element arm 508 or 510 extends through the opening 518, the teeth 520 grip the material of the support part element arm 508 or 510 by friction, and the support part element 501 and the extension part element (504 or 506). Provides an adjustable (one-way) connection between The teeth 520 are shaped such that the support element arm 508 or 510 moves through the opening 518 in the adjustment direction and prevents movement through the opening 518 in the opposite direction, the ends of the teeth 520 being in the adjustment direction Are oriented and inclined to frictionally engage the material (eg, mesh) of the support sub-element arm to allow movement and prevent movement in the opposite direction. By allowing movement in only one direction, the friction adjustment element 512 allows for one-way adjustment of the length of the extensions (503 and 505) of the implant 500.

  FIG. 6 shows in cross-section another friction adjustment element 524 according to the invention. The friction adjustment element 524 includes a body 526, an opening 528, and a plurality of teeth 530. As shown, the end of the tooth 530 is spaced from the body portion 531 to form an opening 528. When used, the opening 528 can receive an element of the implant, such as, for example, a support section element arm or an elongated section of an extension section element, and the teeth 530 grip this element by friction, Provides an adjustable connection in one direction between the friction adjustment elements. The teeth 530 allow the implant element to move through the friction adjustment element 524 in the adjustment direction, but prevent the implant element from moving through the friction adjustment element 524 in the opposite direction.

  FIG. 7 shows an embodiment of a friction adjustment element 522 that includes a guard 532 to allow for two-way adjustment of the length of the implant extension. Friction adjustment element 522 includes a body, openings, and teeth 528, and implant elements (e.g., elongated elements of the extension portion) extend through the openings and engage teeth 528 as shown. Or movement in two directions can be prevented. The guard 532 includes a body 534 and teeth 536 that engage and cooperate with the teeth 528 of the friction adjustment element 522. When the guard 532 meshes with the friction adjustment element 522, the elements of the implant extension (not shown) that extend through the opening of the friction adjustment element 522 in contact with the teeth 528 are in both directions. Can move through 522 and provide bi-directional adjustability. This is because the teeth 528 of the friction adjustment element 522 are covered by the guard 532, thereby preventing the teeth 528 of the friction adjustment element 522 from engaging the elements of the extension. When the guard 532 is removed or disconnected from the friction adjustment element 522, the teeth 528 engage the elements of the extension portion, so that the elements of the extension portion in relation to the friction adjustment element 522 ( Hinder movement (in at least one direction). To facilitate removal of the guard 532 from the friction adjustment element 522 at a desired time, a suture (shown in FIG. 7) or the like is attached to the guard 532 as shown. It is preferable.

  FIG. 8 shows a typical adjustable pelvic implant 730. The implant 730 includes a support portion element 732 that includes a support portion element arm 734. The extension subelement 736 is adjustably connected to the support subelement arm 734 by a friction adjustment element 738. The length of the extension 741 composed of the support part element arm 734 and the extension part element 736 is adjusted (shortened) in one direction by pulling the end 745 through the friction adjustment element 738 in the direction of the arrow. Can do. The support part element arm 734 cannot move through the friction adjustment element 738 in the opposite direction. A tissue fastener (eg, self-fixating tip) 740 is located at the distal end of the extension segment 736.

  As shown, the support subelement arm 734 includes a suture 742 that forms a releasable sagging region 743 within the support subelement arm 734. When used, the friction adjustment element 738 provides a pulling function, while the suture 742 provides a loosening function that can add length to the extension 741 and allows a one-way adjustment of friction. The extension 741 can be shortened by pulling the end 745 through the adjustment element 738 and, if necessary, the extension 741 can be extended by cutting the suture 742 to release the slack 743. Can do. Thus, the implant 730 has a one-way adjustment function to reduce the length of the extension portion 741 and another function to extend the extension portion 741 after using the one-way adjustment function as needed or required. And including.

  When used, embodiments of the implants of FIGS. 1-8 (and other implants with adjustable length extensions) can be used for pelvic tissue (e.g., any pelvis described herein). Can be implanted according to a method comprising the step of placing a tissue support portion of the implant in a position to support the tissue. Next, one or more extensions are structurally disposed to support the tissue support portion. For example, the tissue fastener at the distal end of the extension may be placed in the internal tissue of the pelvic region, such as muscle, ligament, tendon, fascia, bone, or through the tissue in the pelvic region toward the outer incision. Can do. The length of the adjustable extension can be adjusted to adjust the position of the tissue support portion or to adjust the tension applied to the adjustable extension when supporting the tissue support portion.

  Implantation can be performed, for example, transvaginally (for female construction) or perineally (for male construction) through the inner incision and engaged with the distal end of the extension, such as by engagement with a tissue fastener. This can be done by using a matching insertion tool (eg, any insertion tool described herein). When placing the distal end of the extension portion and the tissue support portion, the length of the extension portion is shortened or extended by moving the element of the extension portion relative to the frictional adjustment element, and the position or support of the support portion. The tension applied to the part can be adjusted.

  1 and 2, the friction adjustment element can be secured to the proximal end of the extension element and the elements of the support element arm extend through the opening of the friction adjustment element. be able to. The adjustment can be carried out by adjusting the amount (in terms of length) of the support part element arm that extends through the opening of the friction adjustment element. This generally affects the length of the material that extends between the support portion and the distal end of the extension, eg, the attached self-fixating tip. According to another embodiment of the implant, the friction adjustment element can be fixed to the support part element, for example with a tissue support part or a support part element arm, and the element of the extension part element passes through the opening of the friction adjustment element. Can be extended. The adjustment can be performed by adjusting the amount (in terms of length) of the extension element extending through the opening of the friction adjustment element.

  A typical friction adjustment element 512 provides one-way adjustability, and a typical friction adjustment element 522 provides two-way adjustability. When the element of the support subelement arm is pulled through the friction adjustment element 512, the teeth of the friction adjustment element prevent the support subelement arm from moving through the friction adjustment element in the opposite direction. In contrast, the friction adjustment element 522 (along with the installed guard 532) allows the elements of the support sub-element arm to move through the friction adjustment element in both directions until the guard 532 is removed. Once the desired placement and tension of the implant is selected, the guard 532 can be removed to maintain the desired placement and tension.

  The extension 741 of the implant 730 shown in FIG. 8 can provide unidirectional or bi-directional accommodation. In use, adjustment is performed by the friction adjustment element 738. If desired, the suture 742 can be cut to release the slack in the support portion element arms and readjustment can be performed by the friction adjustment element 738.

  FIG. 9 shows a multi-element implant or a portion of a multi-element implant that includes a friction adjustment element 544, which is the engagement of the implant element extending through the opening of the friction adjustment element 544 and the teeth of the friction adjustment element 544. It has a sheath 546 that selectively prevents or allows bonding. Referring to FIG. 9, the support portion element arm 540 is shown adjustably connected to the extension portion element 542 by a friction adjustment element 544. Friction adjustment element 544 may be a friction adjustment element as described herein, or a friction adjustment element that engages by any similar friction. The frictional adjustment element 544 can be attached to the proximal end of the extension portion element 542 and the elements of the support portion element arm 540 are received by the friction adjustment element 544. The extension portion element 542 also includes a tissue fastener (eg, a self-fixating tip) 541 at the distal end. As shown, a film extension 548 of the sheath 546 is disposed between the teeth of the support subelement arm 540 and the friction adjustment element 544. The film extension 548 prevents the friction surface (such as teeth) of the friction adjustment element 544 from frictionally engaging the mesh material of the support element arm 540. The support portion element arm 540 can move through the friction adjustment element 544 in either of two directions as long as the film extension 548 of the sheath 546 is in this described position. When the desired position of the implant is achieved, the sheath 546 and the film extension 549 are removed and the friction surface (eg, teeth) of the friction adjustment element 544 engages the material of the support subelement arm 540 to position it. Can be maintained.

  Referring to FIG. 9A, the sheath 546 preferably includes a body 547, a film extension 548, and a suture 550. As shown, the sheath 546 includes a proximal end configured as a tube or skin having two sides disposed around and capable of covering the support portion element arms of the support portion element. . Extending from the distal end of the tube or skin is a single film sheet (extension 548) that can be inserted to pass through the opening of the frictional adjustment element 544 with the elements of the implant. The extension 548 can be disposed between the friction surface of the friction adjustment element 544 and the material of the implant element (eg, a support part element arm), which arrangement moves the implant element in two directions for adjustment. Allow that. After adjustment, the extension 548 can be removed to allow frictional contact between the friction adjustment element 544 and the implant element to prevent movement. The use of a one-sided extension (548) that passes through the opening of the frictional adjustment element 544 (instead of a two-sided sheath) reduces the amount of material that will pass through the opening, thereby adjusting Reducing the force required to move the support element arm 540 through the friction adjustment element 544.

  Referring to FIG. 9, the sheath 546 also preferably includes a suture 550 connected at a point along the length of the sheath 546. The suture 550 can be heat staked or joined to the sheath 546 at one or more locations along the length of the sheath 546. The suture 550 extends a certain length away from the sheath 546 and, when used, stays in a position (eg, outside the patient or outside the inner incision) to allow the suture Can be used to facilitate the placement and removal of the sheath. The suture 550 can also be used as a guide for the physician's heel to reach the frictional adjustment element 544 and cut excess material extending through the frictional adjustment element 544.

  In use, a tissue fastener 541 located at the distal end of the extension 542 is used to secure the distal end of the extension shown to the internal tissue of the pelvic region. After some time after the fasteners 541 have been placed, the sheath 546 can be cut along its length to remove the sheath. Removal of the sheath 546 and extension 548 exposes the support subelement arm 540 to the teeth of the friction adjustment element 544. At any step, the physician can use suture 550 to guide the heel and trim away excess material in support portion element arm 54 that extends through frictional adjustment element 544.

  FIG. 10 shows another exemplary multi-element pelvic implant (586). In this embodiment, the unidirectional friction adjustment element is fixed to the support portion element, and the element of the extension portion element is adjustably engaged with the friction adjustment element. The implant 586 includes a support portion element 588 that includes friction adjustment elements 590 and 592. Friction adjustment elements 590 and 592 include openings through which elements of extension 594 pass. A plurality of teeth are arranged to contact the elements of the extension portion 594 that pass through the opening so that the elements of the extension portion element move in one direction through the friction adjustment element 590 and in the opposite direction. Then let's resist movement.

  Extension portion element 594 is shown adjustably connected to friction adjustment element 590. The elements of extension portion element 594 extend through friction adjustment element 590 and a tissue fastener (eg, self-fixating tip) 596 is disposed at the distal end of extension portion 594. Friction adjustment elements 590 and 592 may be extended by adjusting the amount of extension portion element 594 extending through friction adjustment elements 590 and 592 as shown to adjust the length of the extension portion of implant 586. The partial element 594 moves through the friction adjustment element in one direction and resists movement in the opposite direction.

  Implants such as those shown in FIGS. 10 and 11 can be adjusted using an adjustment tool that assists in moving one or more portions of the implant in relation to each other after being implanted. A typical adjustment tool 598 is shown in FIGS. Tool 598 includes an opening 600 at the distal end of tool 598 for receiving extension 594 as shown. In use, when the self-fixating tip 596 is anchored in tissue, the tool 598 moves into the extension portion element 594 in the adjustment direction 602 until the distal end of the tool 598 contacts the friction adjustment element 590. Can slide along. The distance between the self-fixating tip 596 and the support portion element 588 can then be adjusted to reduce the length of the extension portion of the implant 586 by further moving the adjustment tool 598 in the adjustment direction 602. .

  As shown in FIGS. 10 and 11, the opening 600 at the distal end of the tool 598 is sized to receive the material of the extension portion element 594 and to engage the surface of the friction adjustment element 590. It has a round opening. Accordingly, the diameter of the opening 600 is greater than the outer diameter of the friction adjustment element 590 such that the surface of the distal end of the tool 590 surrounding the opening 600 engages the surface (eg, flange) of the friction adjustment element 590. small.

  FIGS. 12 and 13 show another embodiment of an adjustment tool 604 and 606 useful for adjusting the length of an extension portion of an implant, such as implant 586. Tool 604 is slidable over an extension (eg, a mesh support portion element arm), for example, the length of the extension portion of implant 586, such as the distance between tissue fastener 596 and the tissue support portion of support portion element 588. An open slot 608 is included at the distal end of tool 604 that can be used to adjust the thickness. Tool 606 includes an opening 610 and a slit 612 at the distal end of tool 606. The opening 610 is designed to function like the opening 600 of the tool 598 (described above), the opening 610 being slidable along the extension and the tool 606 surrounding the opening 610 (or 608). The surface of the distal end of (or 604) engages the surface (eg, flange) of a friction adjustment element (not shown) to provide extension length adjustment. The slit 612 allows the extension portion to be fed into the opening 610 at a desired location along the length of the extension portion.

  A tool 614, another embodiment of an adjustment tool, is shown in FIG. The tissue support portion or support portion element 616 includes a friction adjustment element 618 (in one direction). The extension portion element 620 is adjustably connected to the friction adjustment element 618. The extension portion element 620 is connected to the tissue by a tissue fastener (eg, self-fixating tip) 622 at the distal end of the extension portion element 620. The adjustment tool 614 includes a flexible or rigid tube that slides over the extension portion element 620 as shown. End 624 of tool 614 is engageable with a surface (eg, flange) of friction adjustment element 618 and tool 614 is adjusted to adjust the distance between support portion element 616 and self-fixating tip 622. Can move along direction 626.

  10A and 10B illustrate a typical multi-element pelvic implant (486). In these embodiments, the friction adjustment element is movably engaged along an extension portion element extending through the opening of the support portion element, and by moving the arrangement of the friction adjustment element, for example, the support portion The length of the extension, measured to be the length between the element and the distal end of the extension element, can be adjusted (eg, in the adjustment direction toward opening 492).

  Implant 486 includes support portion element 488 with loose openings (eg, grommets or openings) 490 and 492. The extension 494 loosely penetrates the respective openings 490 and 492 and allows movement in two directions. By placing a friction adjustment element 496 in the element of the extension 494 that is adjustable in at least one direction, and preferably adjustable in one direction and non-adjustable in the other direction, The adjustment element 496 is moved along the element of the extension 494 closer to the support portion element 488 and the length between the friction adjustment element 496 and the fastener 486 (using the one-way friction adjustment element 496 is used). Or can be reduced and extended (using a two-way friction adjustment element 496). For example, the opening 442 and the element of the extended portion element 484 that penetrates the friction adjustment element 496 can be pulled in one direction through the opening 442 and the friction adjustment element 496 and resist movement in the opposite direction. can do.

  In use, the support sub-element 488 can be positioned and adjusted at a desired location to support the tissue. The self-fixating tip 486 can be placed at a desired location. To maintain the desired position of the support portion element 488, the friction adjustment element 496 is moved or slid along the extension portion element 494, eg, toward the self-fixating tip 486. This can be performed using the adjustment tools described herein. By moving the extension portion element 494, the length of the extension portion element 494 between the opening 442 and the self-fixating tip 486 can be adjusted and fixed, and the anatomical position of the support portion element 488 can be adjusted and maintained. .

  FIGS. 10A and 10B show the openings 490 and 492 of the support portion element of the implant, along with the elements of the elongated extension portion element (494) passing through the opening 492. FIG. In another embodiment, the configuration is similar except that the opening can be arranged on the support subelement in a different manner, such as the distal end of the elongate support subelement arm, etc. Can be. In yet other embodiments, a loose opening can be disposed in the extension portion element (eg, at the proximal end of the extension portion element) and is an extension that is part of a support portion element, eg, a support portion element arm. The elongate element of the portion can pass through the loose opening and the frictional adjustment element can be movably arranged at a position distal from the opening 492 to the support portion element arm, e.g., to the tissue support portion By moving the frictional adjustment element along the support part element arm toward the extension part of the implant by changing the amount of the support part element extending through the friction adjustment element past the opening in the extension part element The length of can be adjusted.

  FIGS. 10, 10A, and 10B show various shapes of an implant having two legs and a tissue support portion. The adjustable extension shown in these figures may be any implant, such as an implant having four, six, or any other number of extensions and having any shape of tissue support. Can be used with. Also, the self-fixating tip 486 may not be present or may be replaced by any other type of tissue fastener. The support portion element 488 is shown as a biological material, but may be a synthetic material. The extension subelement 494 (and band 489) is shown as a synthetic mesh.

  FIGS. 15-21 illustrate various embodiments of a method for securing a frictional adjustment element to an implant (eg, to an extension part element or to a support part element with a tissue support part or support part element arm). Yes. FIG. 15 shows a perspective view of an implant 627 comprising a “grommet style” frictional adjustment element 628 secured to a biological material 630. FIG. 16 is a cross-sectional view. As shown, the friction adjustment element 628 includes a central opening 632, a first flange 634, a second flange 636, and a plurality of flaps or “teeth” 638 that extend in the direction of the opening 632. In an exemplary embodiment, the external diameter of the friction adjustment element 628 is about 5 mm (eg, 3-10 mm) and the length of the flap 638 can be in the range of about 1 mm to about 2 mm.

  FIG. 17 shows a perspective view of another exemplary implant 639. FIG. 18 is a cross-sectional view. The implant 639 includes a frictional adjustment element 640 secured to the biological material 642, which can be a support sub-element of the implant. Friction adjustment element 640 includes an opening 644, a first flange 646, a second flange 648, and a plurality of flaps or “teeth” 650 extending from an interior surface 652 of opening 644. The flap 650 is recessed within the opening 644 and does not extend past the first flange 646. In an exemplary embodiment, the external diameter of the friction adjustment element 640 is about 5 mm (eg, 3-10 mm) and the length of the flap 650 can be in the range of about 1 mm to about 2 mm.

  FIG. 19 shows a perspective view of an implant 653 that includes a friction adjustment element 654 that is part of a support portion element arm 661 and a support portion element 656 (biological material). FIG. 20 is a cross-sectional view. Implant 653 includes support portion element arms 661 constructed from first and second portions 658 and 660 of synthetic mesh material (connected to support portion element 656 by rivets 662). Alternatives to rivets include stitching, stitching, bonding, thermal bonding, or combinations thereof. The first and second mesh portions 658 and 660 extend past the end of the biological material 656 and form a support portion element arm 661. Friction adjustment element 654 is disposed at the distal end of support portion element arm 661. Friction adjustment element 654 includes an opening 664 and a flap (eg, “tooth”) 666 extending toward opening 664. Friction adjustment element 654 is similar to friction adjustment element 628 shown in FIGS. 15 and 16. Any of the friction adjustment elements described herein can be used, such as the friction adjustment element 640 shown in FIGS.

  FIG. 21 shows a cross-sectional view of another implant 667 that includes a friction adjusting element 668 and a biological material 670. The implant 667 includes a synthetic mesh support subelement arm 672 connected to a (biological material) support subelement 670 by a rivet 674. The mesh support subelement arm 672 extends past the end of the biological support subelement 670, and the friction adjustment element 668 is disposed toward the distal end of the mesh support subelement arm 672. As shown, the friction adjustment element 668 includes a central opening 676 and a “flap” or “tooth” 678 extending toward the opening 676. As shown, the friction adjustment element 668 is similar to the friction adjustment element 628 shown in FIGS. 15 and 16. Any of the friction adjustment elements described herein, such as the friction adjustment element 640 shown in FIGS. 17 and 18, can be used.

  22-24 show a “multi-layer” or “hybrid” type tissue support portion (or alternatively) composed of two layers, one layer being a synthetic layer and the second being a biological layer (or 1 shows various embodiments of a pelvic implant including a support sub-element). Optionally, the hybrid tissue support portion may be incorporated into an implant as described herein, such as within a support portion section of a multi-element implant that also includes an extension portion and a frictional adjustment element as described herein. Can do.

  In FIG. 22, a portion of a typical pelvic implant 552 is shown in an exploded view. The implant 552 includes a support portion element 553 that includes a tissue support portion 551 and support portion element arms 560 and 562. The tissue support portion 551 includes a synthetic layer 554 made from a synthetic material such as a mesh and a biological layer 556 made from a biological material such as a pig or human cadaver. The mesh layer 554 includes a mesh tissue support portion 558 and first and second support portion element arms 560 and 562. Support sub-element arms 560 can be connected (eg, adjustable) to an extension sub-element (not shown) of the multi-element implant to form multi-element implant 552. As shown, the biological layer 556 generally has the same size and shape as the mesh layer 554 except that it does not include support portion arms 560 and 562. Support sub-element arms 560 and 562 do not contain biological material and are composed of a single layer of synthetic material. Biological layer 556 can be attached to mesh layer 554 by any useful fastener, such as polymeric rivet 564, as shown, or by using stitching, staples, thermal bonding, bonding, and the like. it can. In use, the biological layer 556 can be placed in contact with sensitive tissue, such as vaginal tissue.

  FIG. 23 shows another exemplary hybrid or multi-layer implant. Implant 680 may be useful in treating anterior vaginal prolapse, such as, for example, a cystocele, optionally in combination with symptoms of urinary incontinence. The implant 680 includes a support portion element 682, which includes a tissue support portion 686 made from biological material and first and second mesh bands 683 attached to the support portion element 682 by rivets 692. And 685. Upper or “front” mesh band 683 is attached to support portion element 682 and includes first and second non-adjustable upper mesh extensions 684 and 686, each of upper mesh extensions 684 and 686 as shown. A tissue fastener (eg, self-fixating tip) 694 is provided at the distal end. Upper extensions 684 and 686 treat vaginal prolapse by supporting the anterior portion of implant 680 that can support one or more of the vaginal tissue, bladder neck, or urethra, and optionally, Can be designed to reduce the symptoms of incontinence. Each tissue fastener 694 can be implanted in a closed hole tissue. Alternatively, the upper extensions 684 and 686 can be longer and can reach the retropubic space, the abdominal incision, the pubic bone, or can reach the outer incision of the internal thigh through the closure hole. . The upper extensions 684 and 686 are shown as having a fixed length, but instead may be adjustable as described herein.

  A second mesh band 685 attached to the support portion element 682 includes first and second support portion element arms 687 and 689 that each include a friction adjustment element 696 secured to the distal end. The first and second lower extension elements 688 and 690 have a tissue fastener (eg, self-fixating tip) 694 at their distal ends and are adjustably connected to the friction adjustment element 696 as shown. Yes.

  FIG. 24 shows another exemplary pelvic implant, which is useful for the treatment of posterior vaginal prolapse, such as vaginal tip or vaginal prolapse, intestinal aneurysm, rectal aneurysm, and the like. Implant 698 includes a support portion element 700 that is manufactured from a biological material and substantially constitutes a tissue support portion. A reinforcing mesh band 702, which is also a component of the support subelement, extends across the width of the support subelement 700. The reinforcing mesh band 702 is attached to the support subelement 700 by a polymer rivet 708 and includes first and second support subelement arms 701 and 703. First and second extension partial elements 704 and 706 are connected to the support partial element arms 701 and 703 through a friction adjustment element 710 at the distal end of the support partial element arms 701 and 703. Extension partial elements 704 and 706 also include a tissue fastener (eg, self-fixating tip) 712 at its distal end.

  With regard to implants 680 and 698, synthetic materials that are considered useful for manufacturing support subelements, support subelement arms, extension subelements, and tissue fasteners can be a variety of different plastics or strong and intracorporeal. Other materials that are useful for use in (e.g., biocompatible) can be included. Typical materials are plastics such as polypropylene, polyethylene, cellulose, polyvinyl, silicone, polytetrafluoroethylene, polyglactin, Silastic, carbon fiber, polyethylene, nylon, polyester (eg, Dacron) PLLA, acetol, EPTFE, and PGA, and Thermoplastic materials can be included. The support subelement, or extension subelement, or tissue fastener synthetic implant material can be independently either resorbable, resorbable, or non-resorbable. Optionally, certain implant components can be absorbable and other portions can be non-absorbable.

  In another embodiment, the material used to manufacture the tissue support portion can include a non-synthetic material, or a combination of synthetic and non-synthetic materials.

  Some examples of commercially available synthetic materials are MarleX® (polypropylene) available from Bard, Covington, Rhode, Prolene, available from Ethicon, New Jersey. (Registered trademark) (polypropylene) and Mersilene (polyester terephthalate) hernia mesh, Phoenix, Arizona. L. Gore-TeX® (expanded polytetrafluoroethylene), available from Gore and associates, American Medical Systems, Inc., Minnetonka, Minnesota. Polypropylene slings provided in the SPARC® sling system available from the company. Commercially available examples of absorbable materials include Dexon® (polyglycolic acid) available from Davis and Geck, Inc., Danbury, Connecticut, and Vicryl (registered) available from Ethicon. Trademark).

  The present invention also relates to an insertion tool that is useful for placing an implant. FIGS. 25 and 26 show a driver 714 placed on a finger 715 of a user (eg, a surgeon). The insertion tool 714 includes a rigid, semi-rigid, or flexible sheath 716, such as a finger cover, sheath, or finger “sack” that is distal to the sheath 716 at a reinforced portion 720 of the sheath 716. A distal end 718 is provided at the end. A typical finger sack can be composed of a flexible elastic material such as natural or synthetic rubber, for example, a flexible material such as butadiene.

  Referring to FIG. 27, an insertion tool 714 is shown in use with a pelvic implant 722. The implant 722 includes a tissue support portion 724, an extension portion 726 extending from the tissue support portion 724, and a self-fixating tip 718 at the distal end of the extension portion 726 (the illustrated extension portion 726 has a fixed length). And does not include a friction adjusting element, but may alternatively include a friction adjusting element). The self-fixating tip 728 includes a surface such as an internal channel that engages the distal end 718. The finger sack 716 can be rigid, semi-rigid, or flexible, and can optionally be supplied in a rolled configuration that can be deployed to a user's finger. The user can advance the self-fixating tip 728 into the tissue and fix the self-fixating tip 728 in a desired position. The insertion tool 714 can then be retracted to separate the self-fixating tip 718 from the distal end 718 of the tool 714.

  Another insertion tool 566 is shown in FIG. The insertion tool 566 is similar to the insertion tool 714 and includes a flexible or non-flexible sheath 568 such as a finger sack with an elongated tip 570 attached to the sheath 568 with a reinforced portion 572. The insertion tool 566 further includes a finger ring 574 that is attached to the sheath 568 through the support portion 576. The finger ring 574 can be adjustable to accommodate different finger sizes. When used, the tool 566 can be used in the same manner as the tool 714 of FIGS. Ring 574 and sheath 568 can be placed on the surgeon's finger so that ring 574 and support portion 576 are useful for providing stability when implanting a self-fixating tip.

  FIG. 29 shows an insertion tool 444 for inserting a self-fixating tip at a deep pelvic location, such as in the ischial spine region, coccyx region, sacrospinous ligament, tendon arch region, and the like. The insertion tool 444 includes a handle 446 attached to a curved shaft 445. Curved shaft 445 extends toward bend 453 followed by a distal end 449 for receiving a self-fixating tip 450 attached to extension 452. Optionally, the position of the end 448 and the self-fixating tip 450 can be maintained by a friction fit between the end 449 and the self-fixating tip 450.

  As shown, the curved shaft 445 includes a curved element that extends between a proximal end attached to the handle 446 and a distal end toward the bend 453. Curved shaft 445 has a length L, which can consist of a combination of curved and straight sections with a total length L along the curved and straight portions. In a preferred embodiment, the length L (measured from the handle 446 towards the bend 453) is about 20.8 to about 254 mm (about 2 to about 10 inches), such as 50.8 to 203.2 mm. (2 to 8 inches). The bend or curvature of the shaft 445 can be as desired, for example, gradual or have one or more bends, and has a straight section and either the same or a different radius of curvature. Can include bends or curves. End element 449 may comprise a length of about 0.25 to 1 inch. The length of the end element 449 includes the length of the end 448 designed to engage the self-fixating tip. The length of the distal end 448 is determined by the particular self-fixating tip 450 and is selected for proper fit with the self-fixating tip 450.

  Also, according to certain embodiments, the angle x (formed by the intersection of tangents 454 and 456, which are tangents at the two ends of shaft 445) is 120-150 degrees. For example, 125 to 145 degrees. The angle y, which is the angle between the tangent 456 and the axis of the end element 449, is in the range of 120 to 150 degrees, for example 125 to 145.

  The length of the end element 449 (including the distal end 448) can be selected to allow the self-fixating portion (eg, tip 750) to be inserted into the tissue by the desired maximum depth. . As shown (not to scale), according to one particular embodiment, the angle x is about 132 degrees and the angle of the bend 453 between the tangent 449 and the end element 449 is about 135. Can be degrees.

  A tool 444 that includes a defined angle and length combination can be a deep tissue in the pelvic region, such as tissue of the sacrospinous ligament, tendon arch, coccyx, iliac coccyx, levator ani, sciatic spine, or the like, or A self-fixating tip (e.g., transvaginal) in the vicinity of one of these tissues can be placed.

  When used, the self-fixating tip 450 can be disposed on the distal end 449 of the insertion tool 444. Insertion tool 444 is inserted through a suitable incision (eg, vagina or perineum) such that self-fixating tip 450 is positioned at the desired location for implantation at the end of extension 452. By using the tool 444, force is applied to the self-fixating tip 450, and the length of the end element 449 serves to limit the depth of insertion to the maximum depth. Next, the insertion tool 444 is removed.

  FIG. 29A shows an insertion tool 744 for inserting a self-fixating tip into a deep pelvic location, such as a sciatic spine region, a coccyx region, a sacrospinous ligament, a tendon arch region, or the like. The insertion tool 744 includes a handle 746 attached to a curved or bent shaft that terminates at a distal end 748 to receive a self-fixating tip 750 attached to the extension 752. Optionally, the position of the end 748 and the self-fixating tip 750 can be maintained by a friction fit between the end 748 and the self-fixating tip 750.

  As shown in FIG. 29A, the shaft of the insertion tool 744 includes three straight elements connected by two bends including a first element 745, a second element 747, and a third element 749. In a preferred embodiment, the first element 745 has a handle (within a range of about 2 to about 6 inches), for example, 2.5 to 5 inches (handles 62.5 to 127 mm). The second element 747 (from the first bend 751 to the second bend 753) has a length of about 50.8 to 101.6 mm (about 2-4). Inches), for example, 63.5 to 88.9 mm (2.5 to 3.5 inches), and the third element 749 has a length of about 6.35 to 25.4 mm (about 0.25 to 1). Inches). The length of the third element 749 includes the length of the distal end 748 designed to engage the self-fixating tip. The length of the distal end 748 is determined by the particular self-fixating tip 750 and is selected for proper fit with the self-fixating tip 750.

  The length of the elements connected by a bend or curve can be measured from the center of the bend or curve. The lengths of elements 745 and 747 connected by bend 751 can be measured from the center of bend 751. The length of elements 747 and 749 can be measured from the center of bend 753.

  According to a preferred embodiment of the tool, the angle of the bend 751 between the first element 745 and the second element 747 is in the range of 120 to 150 degrees, for example 125 to 145 degrees. The angle of the second bent portion 753 between the second element 747 and the third element 749 is in the range of 120 to 150 degrees, for example, 125 to 145. The radius of curvature of the bent portion 751 is a desired one such as in the range of 6.35 to 25.4 mm (0.25 to 1.0 inch), for example, 10.16 to 20.32 mm (0.4 to 0.8 inches). The radius of curvature of the bent portion 753 can be as desired, such as in the range of 2.54 to 12.7 mm (0.1 to 0.5 inches).

  The length of the third element 749 (including the distal end 748) can be selected to allow the self-fixating portion (eg, tip 750) to be inserted into the tissue by the desired maximum depth. As shown (scale is not accurate), according to one particular embodiment, the angle of the bend 751 between the first element 745 and the second element 747 is approximately 132 degrees, and the second element 745 And the angle of the bend 753 between the third element 749 can be about 135 degrees.

  Tools such as tool 744 with the described angle and length combinations are deep in pelvic areas such as sacrospinous ligaments, tendon arches, coccyx, iliac coccyx, levator ani, sciatic spines, etc. Transvaginal placement of the self-fixating tip of the tissue can be achieved.

  When used, a self-fixating tip 750 can be placed on the distal end 748 of the insertion tool 744. The insertion tool 744 can be inserted through an inner incision (eg, vaginal or perineal) such that the self-fixating tip 750 is positioned at the desired pelvic location for implantation at one end of the extension. By using the tool 744, force is applied to the self-fixating tip 750, and the length of the third element 749 serves to limit the depth of insertion to the maximum depth. Next, the insertion tool 744 is removed.

  FIG. 30 illustrates a medial incision (eg, vaginal or perineal incision) of deep pelvic tissue such as or near the sacral ligament, tendon arch, sciatic spine, or the coccyx or iliac coccyx or levator ani muscle. ) Shows another insertion tool 754 for implanting a self-fixating tip through The insertion tool 754 includes a handle 756 and a shaft extending from the handle 756 to the distal end 758 for receiving a self-fixating tip 760 attached to the distal end of the pelvic implant 762. The insertion tool 754 includes a first element 755 and a second element 757. In a preferred embodiment, the first element 755 has a length within the range of about 2 to about 8 inches, for example, 6 to 127 mm (2.5 to 5 inches). The second element 757 may have a length of about 2-8 inches (eg, about 50.8-203.2 mm), for example, 3-5 inches (76.2-127 mm). it can. The length of the end 758 depends on the particular self-fixating tip 760 and can be selected for a proper fit with the self-fixating tip 760. An angle 759 between the first element 755 and the second element 757 is in the range of 120 to 150 degrees, for example, 125 to 145 degrees.

  When used, a self-fixating tip 760 can be placed on the distal end 758 of the insertion tool 754. An insertion tool 754 is inserted through the inner incision (eg, the vagina for women or the perineum for men) so that the self-fixating tip 760 can be fixed at the desired pelvic tissue location. By using the tool 754, a force is applied to the self-fixating tip 760 to the desired depth and then the insertion tool 744 is removed.

  FIG. 31 shows another embodiment 764 of an insertion tool that is a tool for securing a pelvic implant at or near a tendon arch or deep tissue within the pelvic region, such as the region of the sciatic spine. The insertion tool 764 includes a handle 766, a shaft 765, a loop 767 at the distal end of the shaft 765, and an end 768 at the end of the loop 767. The loop 767 is useful for positioning the distal end of the implant at or near the tendon arch, such as by allowing the distal end of the extension portion to pass at least partially or completely around the tendon arch. It is. Preferably, the length of element 765 is in the range of about 4 to 9 inches, and the diameter of loop 767 is about 0.32 to 33.02 mm (about 0.33). ˜1.3 inches), for example, 10.16 to 25.4 mm (0.4 to 1 inch). As shown in FIG. 32, an insertion tool 764 can be used to place the distal end 770 of the extension around the tendon arch 769 so that the implant 772 can be taut.

  FIGS. 33-36 illustrate insertion to secure a pelvic implant at deep tissue in the pelvic region, such as by placing the distal end of the extension at or near the tendon arch or in the region of the sciatic spine. Tool 774 is shown. The insertion tool 774 includes a handle 776, a shaft 777, a loop portion 779 pivotally connected to the distal end of the shaft 777 at a pivot point 780, and a distal end 778 of the end of the loop portion 779. End portion 778 receives distal end 782 of implant 784. In use, the insertion tool 774 is used to place the distal end 782 around the tendon arch 783 as shown in FIGS. The implant 784 can then be secured in a correspondingly taut state, for example, by using an adjustable extension with a friction adjustment element.

  According to preferred embodiments and methods, as insertion tool 774 is pushed along direction 786, loop portion 779 and end 778 pivot at pivot point 780, resulting in distal end 782 turning. Pass around the tendon arch 783. The loop portion 779 is preferably connected to the shaft 777 so that the desired control and mobility of the loop portion 779 around the tendon arch 783 can be achieved. For example, the insertion tool 774 may include a spring, linkage, lever, actuator, or the like to provide the desired function and control of the loop portion 779 by the user by operating a control mechanism disposed on the handle 776, etc. Additional mechanical and structural functions can be included. As an example, mechanical linkage can connect loop portion 779 to the proximal end of a tool, such as handle 776, in which case the control mechanism (eg, trigger) is centered about pivot point 780. Control the position of the loop portion 779.

  FIG. 37 secures a pelvic implant to tissue in the pelvic region, such as a tendon arch, sacrospinous ligament, coccyx muscle, iliac coccyx muscle, levator ani muscle or near pelvic tissue in or near the area of the sciatic spine An insertion tool 788 for doing this is shown. Tool 788 includes a handle (not shown) that is operatively connected to cannula 790 and (separately) memory shape wire 792 that can slide while positioned within cannula 790.

  The shape memory wire 792 has a first configuration (“natural shape”) and can be bent into a second shape. In the first configuration, the distal end of the extension portion is attached to the distal end of the cannula 790. When the first configuration is extended from the end of the cannula 790, the arrangement of the distal end of the tissue in the pelvic region can be smoothly performed. It can be. The first configuration may be different from the configuration of cannula 790, and cannula 790 may be straight or curved in two or three dimensions.

  In use, the distal end of wire 792 can be placed within the distal end of cannula 790, in which case the distal end of wire 792 is straight to the distal end of cannula 790. Bends to fit a flat or curved form. The distal end of the wire 792 can then be extended from the distal end of the cannula 790, thus allowing it to take a natural form that can be curved in one or two dimensions. The material of wire 792 needs to be strong enough to be useful to function as part of an insertion tool useful in the described surgical procedure. An example of such a shape memory material is a material called Nitinol, which is a common registered trade name for NiTi alloys including nickel (Ni) titanium (Ti) materials. Advantageously, any of these materials can provide a higher level of fatigue resistance than that of a linear elastic material.

  As shown in FIG. 38, using the insertion tool 788, place the self-fixating tip 796 at a desired location within the pelvic region (not shown) or, for example, the pelvic region around it. Can do. Cannula 790 can be attached to a handle (not shown) at the proximal end of tool 788 and wire 792 moves longitudinally within cannula 790, such as by a control mechanism disposed on the handle (eg, Sliding). As the wire 792 is pushed through the cannula 790, the distal end of the wire 792 extends from the distal end of the cannula 790, resulting in a curved path formed by shape memory (ie, "Natural shape"). The wire 792 has a two-dimensional shape so that when it extends out from the distal end of the cannula 790, the wire 792 produces a two-dimensional or three-dimensionally curved tissue path as shown in FIG. Alternatively, a natural shape that is three-dimensionally curved can be provided. The self-fixating tip 796 of the implant 798 can be pushed through the tissue pathway (eg, rotating around the tendon arch) and thus implanted into the tissue behind the tendon arch.

  FIG. 39 shows another form (800) of a tissue fastener that is a tissue clamp according to the present specification useful for securing the distal end of the extension with tissue in the pelvic region. Tissue clamps are useful for attaching the distal end of the extension to tissue that is not suitable for insertion of a self-fixating tip or “soft tissue anchor”. For example, tissue in the region of the sciatic spine may be shallower than other tissue in the pelvic region, thus allowing for easier tissue clamp attachment than insertion of a soft tissue anchor.

  Referring to FIG. 39, a tissue clamp 800 is shown in an open or unlocked shape. FIG. 40 shows the tissue clamp 800 in a closed or locked configuration. 41 and 42 show schematic plan views of the open and closed shapes.

  Using tissue clamp 800, for example, in the region of the sciatic spine, extended against tissue in the pelvic region such as ligaments such as tissue, tendons, muscles, fascia, etc. that are relatively unsuitable for attachment by use of soft tissue anchors One end of the part can be fixed. In general, tissue clamp 800 includes a moveable arm or jaw that includes a plurality of teeth that can penetrate tissue, and after penetrating, closes and optionally locks the arm or jaw. A tissue clamp 800 can be secured to the tissue.

  The term “tissue clamp” as used herein refers to a clamp, such as clamp 800, that is useful for attaching to tissue in the pelvic region. As shown, the tissue clamp 800 includes first and second clamp arms 802 and 804 that are pivotally connected by a pivot axis 806. The first clamp arm 802 includes teeth 808 and 810 that can grip tissue when the tissue clamp 800 is installed. The second clamp arm 804 includes teeth 812 that fit between teeth 808 and 810 in a closed configuration, as shown in FIG. Additional teeth can be used with either clamp arm.

  A clamp, such as clamp 800, can be prepared from any suitable material, such as surgical metal, ceramic, or plastic, that is sufficiently hard and strong to be useful in this type of application.

  The tissue clamp 800 can be secured to the distal end of the extension by any fastening configuration. Also, as shown, the first and second clamp arms 802 and 804 also include openings 814 and 816, either or both of which can be used to attach the clamp 800 to an extension of a pelvic implant (not shown). Can be attached to the distal end. Other mounting configurations such as adhesives and metal crimps can also be used.

  The first and second clamp arms 802 and 804 also include optional locking tabs 818 and 620 that, when installed, function to lock the clamp arms 802 and 804 in the closed position. Each locking tab 818 and 820 includes at least one locking tooth engagement that cooperates with an opposing structure (eg, locking tooth or ridge) to lock the tissue clamp 800 in a closed configuration similar to a hemostatic forceps.

  The dimensions of the tissue clamp can be any useful size, for example, can be relatively small, such as in the same range as the dimensions of the self-fixating tip. In an exemplary embodiment of the tissue clamp 800, the overall length 801 of the closed shape tissue clamp 800 may be about 1 cm, for example, about 0.5 cm to about 1.2 cm. Also, in the closed configuration, the distance from pivot axis 806 (measured along the longitudinal axis parallel to line 801) to one end or tip of the jaw may be about 3 mm, for example about 2 ~ About 6 mm. Preferably, the angle α between the jaw and the tooth may be about 30 degrees, for example about 20 to about 50 degrees.

  When used, areas for attaching tissue clamps, such as tissue clamp 800, include internal obturator muscles, coccyx muscles, iliac caudal muscles, anal lifts to treat vaginal prolapse, urine stress incontinence, and fecal incontinence. It can include muscle, pubic rectal muscle, sciatic spine, levator ani muscle, sacrospinous ligament region, and levator ani tendon arch.

  FIG. 43 shows an extension 832 that can be used with a pelvic implant according to the present description. The extension 832 can optionally be part of an extension part element or part of a support part element arm of a multi-element implant. The extension 832 includes a biocompatible mesh material and one or more releasable mesh folds 834 (only one is shown), each of which has a suture 836. It is fixed by. If used, if desired, one or more of the sutures 836 can be cut to release one or more folds and the extension portion 832 can be extended. The mesh fold is described herein by placing the implant, cutting the suture 836 to release the fold 834, and extending the extension to adjust the length of the extension, as desired. Can be used in combination with other types of adjustable extensions (eg, including friction adjustment elements).

  FIG. 44 shows an implant 906 that includes a tissue fastener for positioning the distal end of the extension with tissue in the pelvic region. The implants 906 are opposed to each other as shown in FIG. 46 and can be connected to firmly engage each other through soft tissue such as muscle or fascia in the pelvic region, for example. It includes a male connector element 910 (only one is required) and a plurality (only one is required) female connector element 908.

  FIG. 44A shows another embodiment 906 'of an implant that is an implant that includes a tissue fastener for positioning the distal end of the extension in tissue of the pelvic region. The implants 906 ′ are opposed to each other as shown in FIG. 46 and can be connected to firmly engage each other through soft tissue such as muscle or fascia in the pelvic region, for example. It includes a male connector element 910 (only one is required) and a plurality (only one is required) female connector element 908. The implant 906 ′ includes an auxiliary extension 907 that extends from the main extension 909. Each of the auxiliary extension 907 and the main extension 909 includes a female or male connector element.

  In general, a male friction adjustment element (eg, 910) can be inserted into opposing female friction adjustment elements (eg, 908) and the surfaces of the two opposing connector elements are separated from each other by the male and female connector elements. To prevent. Any, including grooves, ridges, holes, flanges, hooks, and the like, which when engaged are frictionally engaged to hold the female connector element firmly to the male connector element Female and male connector elements that engage each other can be used. The opposing female and male connector elements are such that when the female and male connector elements are pressed together with the tissue disposed between the male and female elements, the male elements engage the female elements. It must also have the ability to penetrate tissue such as muscle or fascia in a manner that allows for this.

  FIG. 45 shows an installation tool 912, which is a tool for installing the implant 906 or 906 '. The installation tool 912 includes tool arms 914 and 916 that pivot about a pivot axis 918. Tool arms 914 and 916 include jaws 920 and 0922, respectively. The jaws 920 and 922 include structures for holding the elements 908 and 910 for engaging and placing the male and female connector elements 908 and 910 in tissue. With the tissue positioned (or “sandwiched”) between the male and female connector elements 910 and 908, the jaws 920 and 922 can be positioned at the desired tissue location. The tool 912 is then used to drive the male connector element 910 through the tissue and into each other toward the female connector element 908 and into the interengaged state at the selected tissue location. The distal end of the extension is held against pelvic tissue. Such an action bites or clamps a portion of tissue between the implants 906 to lock the implant 906 in place.

  FIG. 45 shows an insertion tool 912 that holds male and female connector elements 910 and 908 for placement in tissue.

  FIG. 46 shows male and female connector elements 910 and 908 that connect the implant 907 to the tissue 907 by being connected together within the tissue 907.

  FIG. 47 illustrates a tissue fastener embodiment 924 that is a self-fixating tip that can be used in combination with an implant or extension. The self-fixating tip 924 can be connected to a pelvic implant (not shown), such as at the distal end of the extension, and can be used to secure the distal end to tissue in the pelvic region. . The self-fixating tip 924 includes a housing portion 926 with a tip 927 and a wire 928 connected to a deployable barb 930 that passes through an opening 931 in the housing portion 926. The self-fixating tip 924 can be designed such that the barbs 930 are deployed by moving the wire 928 relative to the housing portion 926.

  The barbed 930 can be designed to be deployed by a spring force or the like of the barbed material when advanced in the direction 929. That is, the barbs 930 can be held in the housing portion 929 until the barbs 930 are advanced by spring force after the barbs 930 have advanced toward the opening 931.

  In another embodiment, barbs 930 can be designed to be deployed in the case of parallel movement of wire 928 in the opposite direction of direction 929. According to this design, the barbed 930 is pre-arranged and installed in the vicinity of the opening 931 such that the reverse barb 930 is deployed through the opening 931 due to the bending of the barbed 930 in the case of parallel movement of the wire 928. be able to.

  In use, the insertion tool 925 can be released while coupled to the self-fixating tip 924. Any cleavable bond can be used, including those including yarn, flange, detent, spring, shoulder, and the like. The insertion tool 925 is used to advance the self-fixating tip 924 to the desired location within the tissue. When positioned as desired, the barbs 930 can be deployed (ie, extended from the housing portion 929) to secure the self-fixating tip 924 to the tissue. The insertion tool 925 is then removed from the self-fixating tip 924 and removed.

  FIGS. 47-49 show another embodiment 932 of a tissue fastener that is a self-fixating tip with an installation tool 942. The self-fixating tip 932 can be connected to a pelvic implant (not shown) and can be used to secure the pelvic implant to tissue in the pelvic region. As shown, the self-fixating tip 932 includes a tube portion 934 disposed within the housing 936. The housing 936 includes a tip 933 and an opening 940. The tube portion 934 includes a slit 938 that forms a barbed 937 with a spring force that can spread outward and extend through the opening 940 when advanced by the installation tool 934.

  The installation tool 942 includes a cannula 944 and a rod 946 that can translate in relation to the cannula along the deployment direction 948 therein. The installation tool 934 also includes a shoulder 950 that engages the shoulder 952 of the housing 936 of the self-fixating tip 932. Other connections such as those including threads, flanges, shoulders, detents, springs, and the like can be used to couple and separate the installation tool 934 and the self-fixating tip 932.

  When used, the insertion tool 934 is coupled to the self-fixating tip 932. The insertion tool 934 is then used to advance the self-fixating tip 932 to a desired location within the tissue. When placed as desired, rod 946 is advanced in direction 948, tube 934 is driven in one or more directions, and barbs 937 are deployed through opening 940 and extended into tissue for self-fixation Tip 932 is secured to the tissue (see FIG. 49). The insertion tool 934 is then separated and removed from the self-fixating tip 932 (see FIG. 50).

  Any of the above-described schematic detailed descriptions of features such as implants, insertion tools, tissue fasteners, and methods may be used in any desired combination to treat female or male pelvic disease. Can do.

  Although the present invention has been described in terms of particular embodiments and applications, those skilled in the art will consider this disclosure and do not depart from or exceed the scope of the claimed invention. Without limitation, further embodiments and modifications can be produced. Therefore, it should be understood that the drawings and the description in this specification are provided as examples for facilitating the understanding of the present invention and should not be construed as limiting the scope of the present invention. .

Claims (14)

A multi-element pelvic implant having a tissue support portion and an extension portion, the implant comprising:
A support portion element having a tissue support portion and a support portion element arm;
An extension element;
Comprising elements including
The support portion element comprises a tissue support portion, at least two support portion element arms extending from the tissue support portion, and a friction adjustment element secured to the support portion element arm;
The extension part element includes two upper extension parts of fixed length and two lower extension parts of adjustable length, the lower extension part being adjustably connected to the support part element; The implant includes a friction adjustment element that adjusts a length of the lower extension portion, the friction adjustment element engaging an opening through which the element of the lower extension portion extends and friction with the element of the lower extension portion. And the frictional engagement preferentially allows movement in one direction of the element of the lower extension through the opening and allows movement in the opposite direction of the element of the lower extension. Prohibit implants. A multi-element pelvic implant having a tissue support portion and an extension portion, the implant comprising:
A support portion element having a tissue support portion and a support portion element arm;
An extension element;
Comprising elements including
The support portion element comprises a tissue support portion, at least two support portion element arms extending from the tissue support portion, and a friction adjustment element secured to the support portion element arm;
The extension part element is adjustably connected to the support part element by a friction adjustment element for adjusting the length of the extension part;
The friction adjusting element is
An opening through which an element of the extension extends,
A surface that frictionally engages the elements of the extension;
With
The friction adjustment element has two configurations, the first configuration allows two-way movement of the element of the extension through the opening, and the second configuration has the surface of the extension portion. An implant that frictionally engages the elements of the extension and prevents movement of the elements of the extension through the opening in at least one direction. A multi-element pelvic implant having a tissue support portion and an extension portion, the implant comprising:
A support portion element having a tissue support portion and a support portion element arm;
An extension element;
Comprising elements including
The extension part element is adjustably connected to the support part element by passing an elongated element of one of the support part element and the extension part element through the other opening;
A friction adjustment element is disposed on the elongate element of the extension portion to allow adjustment of the length of the extension portion, the friction adjustment element comprising an opening through which the elongate element of the extension portion extends, and the extension portion A frictionally engaging surface of the element of the extension portion, wherein the frictional engagement preferentially allows one-way movement of the element of the extension portion through the opening and opposite the element of the extension portion. Implants that prohibit movement in the direction.   The opening is in the support portion element, the proximal end of the extension portion element extends through the opening, and the friction adjustment element is connected to the proximal end of the extension portion element and the support portion. The implant according to claim 3, wherein the implant is disposed in the extension subelement between the opening of the element. The implant according to any one of claims 2 to 4 , comprising a support part and two extension parts. A support portion, and a four extension comprising two lower extensions of the fixed length of two upper extension and adjustable length of, according to any one of claims 2 to 4 Implants. A surgical implant for treating pelvic disease,
The implant comprises a tissue support portion and an extension portion;
The surgical implant wherein the tissue support portion has a plurality of layers of material including a layer of synthetic material and a layer of biological material.   A surgical implant for treating pelvic disease, the implant comprising a tissue support portion, an extension portion, and a tissue clamp at a distal end of the extension portion. A surgical implant for treating pelvic disease, the implant comprising a tissue support portion, an extension portion, and a tissue fastener at a distal end of the extension portion;
The surgical implant, wherein the tissue fastener includes a male engaging element and a female engaging element. A combination of a surgical implant and a tool useful for installing said surgical implant,
The surgical implant comprises a support portion, an extension portion, and a self-fixating tip at a distal end of the extension portion;
A combination wherein the tool comprises a finger sack that can be placed on a finger and a distal end that engages the self-fixating tip. A combination of a surgical implant and a tool useful for installing said surgical implant,
The surgical implant comprises a support portion, an extension portion, and a self-fixating tip at a distal end of the extension portion;
The tool is
A handle,
An elongated curved shaft having a proximal end and a distal end, the proximal end connected to the handle and the distal end connected to an end element through a bend With a shaft,
With
The elongated curved shaft has a length in the range of 6-12 inches (152.4-304.8 mm);
The angle between the tangents at both ends of the curved shaft is in the range of 120-150 degrees;
The bent portion has an angle within a range of 120 to 150 degrees;
The end element has a length of about 0.25 to 1 inch;
The combination wherein the end element comprises a distal end that engages the self-fixating tip. The elongated curved shaft is
A first straight element having a length in the range of 50.8-152.4 mm (2-6 inches);
A second straight element having a length in the range of 50.8-152.4 mm (2-6 inches);
With
12. A combination according to claim 11 , wherein the angle between the tangent at the proximal end of the first element and the tangent at the distal end of the second element is in the range of 125-145 degrees. A combination of a surgical implant and a tool useful for installing said surgical implant,
The surgical implant comprises a support portion, an extension portion, and a self-fixating tip at a distal end of the extension portion;
The tool is
A handle,
An elongate shaft having a proximal end connected to the handle and a distal end connected to a pivoting loop portion, the loop portion having a distal end engaging the self-fixating tip. A combination comprising a shaft. A surgical tool useful for implanting a pelvic implant, the surgical tool comprising:
A handle,
A cannula connected to the handle;
A surgical tool comprising a shape memory wire slidably disposed within the cannula, wherein the shape memory wire has a natural shape different from the shape of the cannula.

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